Page last updated: 2024-10-29

ketamine and Anxiety

ketamine has been researched along with Anxiety in 138 studies

Ketamine: A cyclohexanone derivative used for induction of anesthesia. Its mechanism of action is not well understood, but ketamine can block NMDA receptors (RECEPTORS, N-METHYL-D-ASPARTATE) and may interact with sigma receptors.
ketamine : A member of the class of cyclohexanones in which one of the hydrogens at position 2 is substituted by a 2-chlorophenyl group, while the other is substituted by a methylamino group.

Anxiety: Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS.

Research Excerpts

ExcerptRelevanceReference
"Post hoc data support efficacy of esketamine plus an oral antidepressant in patients with TRD, regardless of comorbid anxiety."9.41The effect of esketamine in patients with treatment-resistant depression with and without comorbid anxiety symptoms or disorder. ( Borentain, S; Daly, EJ; Fedgchin, M; Ionescu, DF; Salvadore, G; Singh, JB; Starr, HL; Thase, ME; Trivedi, MH; Turkoz, I, 2021)
"The N-methyl-D-aspartate receptor antagonist ketamine has rapid onset activity in treatment-resistant depression, post-traumatic stress disorder and obsessive compulsive disorder."9.24Ketamine's dose-related effects on anxiety symptoms in patients with treatment refractory anxiety disorders. ( Anderson-Fahey, B; Glue, P; Gray, A; Harland, S; Le Nedelec, M; McNaughton, N; Medlicott, NJ; Neehoff, S, 2017)
"Patients receiving ketamine for refractory depression and anxiety report dissociative symptoms in the first 60 min post-dose."9.24Effect of ketamine dose on self-rated dissociation in patients with treatment refractory anxiety disorders. ( Castle, C; Glue, P; Gray, A; Neehoff, S, 2017)
" Ketamine has been shown to rapidly and robustly decrease symptoms of depression in depressed patients with bipolar disorder."9.20A single infusion of ketamine improves depression scores in patients with anxious bipolar depression. ( Ionescu, DF; Luckenbaugh, DA; Niciu, MJ; Richards, EM; Zarate, CA, 2015)
"To compare the effects of intranasal midazolam versus different doses of intranasal ketamine on reducing preoperative pediatric anxiety."9.16Comparison of the effects of intranasal midazolam versus different doses of intranasal ketamine on reducing preoperative pediatric anxiety: a prospective randomized clinical trial. ( Adeli, N; Hosseini Jahromi, SA; Hosseini Valami, SM; Yazdi, Z, 2012)
"To compare the effect of low-dose ketamine with that of low-dose fentanyl on patient anxiety during the identification of the epidural space and catheterization."9.09Patient anxiety scores after low-dose ketamine or fentanyl for epidural catheter placement. ( Dohi, S; Iida, H; Oda, A, 2000)
" The ketamine challenge study in schizophrenia subjects is at the vortex of the current debate."9.09The schizophrenia ketamine challenge study debate. ( Carpenter, WT, 1999)
"Ketamine intravenous therapy (KIT) appears effective for treating depression in controlled trials testing a short series of infusions."8.31The effects of ketamine on symptoms of depression and anxiety in real-world care settings: A retrospective controlled analysis. ( Heifets, BD; Hietamies, TM; Klise, AJ; Levine, SP; McInnes, LA; Qian, JJ; Williams, LM; Worley, MJ, 2023)
"Ketamine is a dissociative anesthetic that has been shown to have antidepressant effects in humans and has been proposed as a potential treatment for mood disorders such as posttraumatic stress disorder and aggression."8.31A single dose of ketamine enhances early life stress-induced aggression with no effect on fear memory, anxiety-like behavior, or depression-like behavior in mice. ( Aaflaq, S; Bartsch, CJ; Jacobs, JT; Li, Z; Nordman, JC; Qasem, E; Skinner, S; Smith, M; Summa, F; Thompson, R, 2023)
"One hundred thirty-five Chinese individuals with anxious depression (n = 92) and nonanxious depression (n = 43) received six intravenous infusions of ketamine (0."8.12Antianhedonic effects of serial intravenous subanaesthetic ketamine in anxious versus nonanxious depression. ( Gu, LM; Ning, YP; Tan, JQ; Wang, CY; Yang, XH; Zheng, W; Zhou, YL, 2022)
"Ketamine has emerged as a promising pharmacotherapy for depression and other mental illnesses, and the intramuscular (IM) administration of ketamine is now offered at many North American outpatient psychiatric clinics."8.12Real-world depression, anxiety and safety outcomes of intramuscular ketamine treatment: a retrospective descriptive cohort study. ( Ahuja, S; Brendle, M; Moore, C; Robison, R; Smart, L; Thielking, P, 2022)
" The treatments with ketamine, guanosine, and ketamine plus guanosine were effective to counteract corticosterone-induced anxiety-like phenotype, but not disturbances in the hippocampal NLRP3 pathway."8.02Low doses of ketamine and guanosine abrogate corticosterone-induced anxiety-related behavior, but not disturbances in the hippocampal NLRP3 inflammasome pathway. ( Camargo, A; Dalmagro, AP; Fraga, DB; Kaster, MP; Rodrigues, ALS; Rosa, JM; Zeni, ALB, 2021)
"The aim of this study was to examine the effect on depressive symptoms of repeated subanesthetic doses of SC esketamine in unipolar and bipolar treatment-resistant depression (TRD) and clinical predictors of response."8.02Repeated subcutaneous esketamine for treatment-resistant depression: Impact of the degree of treatment resistance and anxiety comorbidity. ( Abdo, G; B Andreoli, S; B Puertas, C; Barbosa, M; Cohrs, FM; Del Porto, JA; Del Sant, LC; Delfino, R; Fava, VA; Lacerda, AL; Liberatori, A; Lucchese, AC; Magalhães, EJM; Nakahira, C; Sarin, LM; Steiglich, MS; Surjan, J; Tuena, MA, 2021)
"Patients with TRD and prominent anxiety receiving IV ketamine exhibited a significant reduction in depressive, SI and anxiety symptoms."8.02The effectiveness of intravenous ketamine in adults with treatment-resistant major depressive disorder and bipolar disorder presenting with prominent anxiety: Results from the Canadian Rapid Treatment Center of Excellence. ( Gill, H; Ho, R; Kratiuk, K; Lee, Y; Lipsitz, O; Lui, LM; Mansur, RB; McIntyre, RS; Nasri, F; Rodrigues, NB; Rosenblat, JD; Subramaniapillai, M; Teopiz, K, 2021)
"Ketamine has rapid anxiolytic effects in treatment-resistant obsessive compulsive, post-traumatic stress, generalised anxiety and social anxiety disorders."8.02Anxiolytic effects of acute and maintenance ketamine, as assessed by the Fear Questionnaire subscales and the Spielberger State Anxiety Rating Scale. ( Glue, P; Gray, A; Neehoff, S; Nehoff, H; Truppman Lattie, D, 2021)
"Comparison of the S-ketamine group (n = 8; 4 male, 4 female; average age 52 years) with the control group (n = 8; 3 male, 5 female; average age 55 years) revealed a significant multivariate effect on anxiety and depression F(1, 14) = 4."7.96A rapid positive influence of S-ketamine on the anxiety of patients in palliative care: a retrospective pilot study. ( Cordes, J; Falk, E; Grau, I; Kienbaum, P; Lutterbeck, MJ; Neukirchen, M; Schlieper, D; Schwartz, J; van Caster, P, 2020)
"To determine the effectiveness of intravenous (IV) ketamine on anxiety, irritability, agitation, and suicidality, in adults with treatment-resistant major depressive disorder (MDD) or bipolar disorder (BD)."7.96The effectiveness of ketamine on anxiety, irritability, and agitation: Implications for treating mixed features in adults with major depressive or bipolar disorder. ( Cha, DS; Fagiolini, A; Gill, H; Ho, R; Kratiuk, K; Lee, Y; Lin, K; Lipsitz, O; Malhi, GS; Mansur, RB; McIntyre, RS; Nasri, F; Rodrigues, NB; Rosenblat, JD; Subramaniapillai, M; Suppes, T; Vinberg, M, 2020)
"Here we show that mice prenatally exposed to ketamine displayed anxiety-like behaviors during adulthood, but not during puberty."7.96Prenatal Exposure to Ketamine Leads to Anxiety-Like Behaviors and Dysfunction in Bed Nucleus of Stria Terminalis. ( Chen, Y; Feng, X; Guo, H; Hu, Y; Li, Y; Lin, J; Lin, L; Liu, T; Lu, Z; Sun, J; Xu, S, 2020)
"There is scarce information regarding the effects of anesthetic doses of the non-competitive N-methyl-D-aspartate receptor antagonist ketamine on anxiety."7.91Effects of Anesthetic Ketamine on Anxiety-Like Behaviour in Rats. ( Antoniou, K; Delis, F; Georgiadou, G; Pitsikas, N, 2019)
"Ketamine may achieve its effects on treatment-resistant generalized anxiety disorder and social anxiety disorder through related mechanisms to the common reduction by conventional anxiolytic drugs in right frontal theta."7.88Ketamine Effects on EEG during Therapy of Treatment-Resistant Generalized Anxiety and Social Anxiety. ( Glue, P; Kawe, T; Martin, D; McNaughton, N; Neehoff, S; Shadli, SM, 2018)
"The present study characterized the effects of ketamine on sexual behavior and anxiety in female rats."7.88The effects of ketamine on sexual behavior, anxiety, and locomotion in female rats. ( Abdel-Rahim, H; Boyette-Davis, J; DeVore, J; Gonzalez, CMF; Guarraci, FA; Kunkel, MN; Lucero, D; Quadlander, E; Stinnett, M; Womble, PD, 2018)
"This study tested the effects of ketamine on vulnerability of female adolescent mice to activity-based anorexia (ABA)."7.88Single injection of ketamine during mid-adolescence promotes long-lasting resilience to activity-based anorexia of female mice by increasing food intake and attenuating hyperactivity as well as anxiety-like behavior. ( Aoki, C; Chen, YW; Sherpa, AD, 2018)
"We report a case series on the observed effects of low-dose ketamine infusions in 4 critically ill patients with varying complications related to prolonged critical illness."7.83Low-Dose Ketamine in Chronic Critical Illness. ( Darrah, D; Moitra, A; Moitra, VK; Patel, MK; Wunsch, H, 2016)
" Here, two cases are reported in which a single oral dose of ketamine provided rapid and moderately sustained symptom relief for both depression and anxiety."7.76Oral ketamine for the rapid treatment of depression and anxiety in patients receiving hospice care. ( Iglewicz, A; Irwin, SA, 2010)
"It was investigated whether subchronic application of 30 mg/kg ketamine (Ket) induces reliable changes in behaviour and parameters of dopaminergic, glutamatergic, and serotonergic neurotransmissions, which might be the basis of an animal model in schizophrenia research."7.72Ketamine-induced changes in rat behaviour: A possible animal model of schizophrenia. ( Becker, A; Grecksch, G; Huether, G; Mann, T; Peters, B; Schroeder, H, 2003)
"The aim of the present study was to determine the involvement of the median raphe serotonergic system in the effects of ketamine on anxiety behaviours and related memory."7.71Effects of ketamine on different types of anxiety/fear and related memory in rats with lesions of the median raphe nucleus. ( Akman, H; Babar, E; Melik, E; Ozgünen, T; Polat, S, 2001)
" Demographics, adverse events, and patient-reported dissociation were also analyzed."7.11At-home, sublingual ketamine telehealth is a safe and effective treatment for moderate to severe anxiety and depression: Findings from a large, prospective, open-label effectiveness trial. ( Akiki, TJ; Arden, K; Gazzaley, A; Hull, TD; Klotz, M; Madan, A; Malgaroli, M; Paleos, C; Swain, J; Vando, L, 2022)
"About 20 to 30 percent of patients with Major Depressive Disorder (MDD) do not respond to standard treatment and are considered treatment-resistant."6.90Anxiety during ketamine infusions is associated with negative treatment responses in major depressive disorder. ( Aust, S; Bajbouj, M; Basso, L; Chae, WR; Cosma, NC; Gärtner, M; Grimm, S; Heuser-Collier, I; Otte, C; Regen, F; van Hall, F; Wingenfeld, K, 2019)
"Ketamine is a noncompetitive antagonist of the N-methyl-d-aspartate (NMDA) glutamate receptor, which underlies its induction of pain relief and anaesthesia."6.82Ketamine treatment for refractory anxiety: A systematic review. ( Brooks, S; Dahlén, AD; Haggarty, CJ; Schiöth, HB; Tully, JL, 2022)
"Patients with major depressive disorder often have limited response to first-line and second-line medications; hence, novel pharmacological treatments are needed for treatment-resistant depression (TRD)."6.72The Canadian Network for Mood and Anxiety Treatments (CANMAT) Task Force Recommendations for the Use of Racemic Ketamine in Adults with Major Depressive Disorder: Recommandations Du Groupe De Travail Du Réseau Canadien Pour Les Traitements De L'humeur Et ( Beaulieu, S; Blier, J; Blier, P; Brietzke, E; Frey, BN; Kennedy, SH; Lam, RW; McGirr, A; McIntyre, RS; Milev, RV; Parikh, SV; Ravindran, AV; Ravindran, N; Richard-Devantoy, S; Schaffer, A; Swainson, J; Taylor, VH; Tourjman, V; van Ameringen, M; Yatham, LN, 2021)
" The most common treatment-emergent adverse events associated with ketamine/esketamine are dissociation, anxiety, nausea, increased blood pressure, and headache."6.72Prevention and Management of Common Adverse Effects of Ketamine and Esketamine in Patients with Mood Disorders. ( Cao, B; Ceban, F; Chau, EH; Gill, H; Ho, RC; Kratiuk, K; Kumar, A; Lee, JG; Lee, Y; Lin, K; Lipsitz, O; Lui, LMW; Mansur, RB; McIntyre, RS; Nasri, F; Rodrigues, NB; Rosenblat, JD; Subramaniapillai, M; Swainson, J, 2021)
" The control group and the test groups were comparable with regard to biological data, duration of operation, applied dosage of local anaesthetics and actual anxiety before operation."6.68[Analgesia-sedation for maxillo-facial surgery with midazolam-pentazocine and miazolam-ketamine. Clinical double-blind study of anxiety, analgesia, sedation and amnesia]. ( Daubländer, M; Dick, W; Lipp, M; Sebastian, M, 1995)
"Ketamine is a dissociative anesthetic in human and veterinary clinic, as well as an abuse drug that acts on several neurotransmitter systems."5.72Ketamine acutely impairs memory consolidation and repeated exposure promotes stereotyped behavior without changing anxiety- and aggression-like parameters in adult zebrafish. ( Franscescon, F; Michelotti, P; Müller, TE; Pereira, ME; Rosemberg, DB, 2022)
" The higher ketamine use frequency and dosage were associated with more severe depressive symptoms."5.43Profiling the psychotic, depressive and anxiety symptoms in chronic ketamine users. ( Deng, X; Ding, Y; Fan, N; He, H; Ke, X; Ning, Y; Rosenheck, R; Sun, B; Tang, W; Wang, D; Xu, K; Zhou, C, 2016)
"Evidence suggests that clinical markers, such as comorbid anxiety, body weight, and others can assist in predicting response to low-dose ketamine infusion in treatment resistant depression patients."5.41Using classification and regression tree modelling to investigate treatment response to a single low-dose ketamine infusion: Post hoc pooled analyses of randomized placebo-controlled and open-label trials. ( Bai, YM; Chen, MH; Cheng, CM; Hong, CJ; Li, CT; Lin, WC; Su, TP; Tsai, SJ; Tu, PC; Wu, HJ, 2021)
"Post hoc data support efficacy of esketamine plus an oral antidepressant in patients with TRD, regardless of comorbid anxiety."5.41The effect of esketamine in patients with treatment-resistant depression with and without comorbid anxiety symptoms or disorder. ( Borentain, S; Daly, EJ; Fedgchin, M; Ionescu, DF; Salvadore, G; Singh, JB; Starr, HL; Thase, ME; Trivedi, MH; Turkoz, I, 2021)
"Ketamine is a non-competitive N-methyl-D-aspartate receptor antagonist that is Food and Drug Administration-approved in the United States for anesthesia due to its sedative effects with low risk of severe respiratory depression."5.39Two cases of delayed-onset suicidal ideation, dysphoria and anxiety after ketamine infusion in patients with obsessive-compulsive disorder and a history of major depressive disorder. ( Bloch, MH; Corlett, PR; Grunschel, BD; Niciu, MJ; Pittenger, C, 2013)
"Ketamine post-SE onset treatment prevented neuronal death in all regions assessed."5.38Ketamine reduces neuronal degeneration and anxiety levels when administered during early life-induced status epilepticus in rats. ( Córdova, SD; de Oliveira, DL; Loss, CM, 2012)
"Premedication in children with ketamine is useful to produce mild sedation, decrease anxiety, help the child separation from parents, and provide postoperative pain relief with no or little adverse effects."5.34Analgo-Sedative Effects of Oral or Nebulized Ketamine in Preschoolers Undergoing Elective Surgery: A Comparative, Randomized, Double-Blind Study. ( Amin, OAI; Kamel, AAF, 2020)
"To examine the effect of high baseline anxiety on response to ketamine versus midazolam (active placebo) in treatment-resistant depression (TRD)."5.30Efficacy of intravenous ketamine treatment in anxious versus nonanxious unipolar treatment-resistant depression. ( Cusin, C; Debattista, C; Fava, M; Flynn, M; Freeman, MP; Hock, RS; Hoeppner, B; Ionescu, DF; Iosifescu, DV; Mathew, SJ; Papakostas, GI; Salloum, NC; Sanacora, G; Trivedi, MH, 2019)
"The ketamine group was superior to the conventional group which was superior to the no-treatment group in reducing negative affect experienced during stressful situations."5.26Ketamine-facilitated induced anxiety therapy and its effect upon clients' reactions to stressful situations. ( Becker, AT; Corssen, G; Sappington, AA; Tavakoli, M, 1979)
"The N-methyl-D-aspartate receptor antagonist ketamine has rapid onset activity in treatment-resistant depression, post-traumatic stress disorder and obsessive compulsive disorder."5.24Ketamine's dose-related effects on anxiety symptoms in patients with treatment refractory anxiety disorders. ( Anderson-Fahey, B; Glue, P; Gray, A; Harland, S; Le Nedelec, M; McNaughton, N; Medlicott, NJ; Neehoff, S, 2017)
"Patients receiving ketamine for refractory depression and anxiety report dissociative symptoms in the first 60 min post-dose."5.24Effect of ketamine dose on self-rated dissociation in patients with treatment refractory anxiety disorders. ( Castle, C; Glue, P; Gray, A; Neehoff, S, 2017)
"S-ketamine is approved for treatment-resistant patients with depression and adult patients with suicide behavior."5.22Neurobiological, behavioral, and cognitive effects of ketamine in adolescents: A review of human and pre-clinical research. ( Acevedo, J; Siegel, JA, 2022)
" Ketamine has been shown to rapidly and robustly decrease symptoms of depression in depressed patients with bipolar disorder."5.20A single infusion of ketamine improves depression scores in patients with anxious bipolar depression. ( Ionescu, DF; Luckenbaugh, DA; Niciu, MJ; Richards, EM; Zarate, CA, 2015)
"To compare the effects of intranasal midazolam versus different doses of intranasal ketamine on reducing preoperative pediatric anxiety."5.16Comparison of the effects of intranasal midazolam versus different doses of intranasal ketamine on reducing preoperative pediatric anxiety: a prospective randomized clinical trial. ( Adeli, N; Hosseini Jahromi, SA; Hosseini Valami, SM; Yazdi, Z, 2012)
"Midazolam and ketamine are useful for oral premedication in children to allay anxiety."5.15Low- versus high-dose combination of midazolam-ketamine for oral premedication in children for ophthalmologic surgeries. ( Darlong, V; Garg, R; Pandey, R; Punj, J; Shende, D; Singh, M, 2011)
" The ketamine challenge study in schizophrenia subjects is at the vortex of the current debate."5.09The schizophrenia ketamine challenge study debate. ( Carpenter, WT, 1999)
"Our understanding of depression and its treatment has advanced with the advent of ketamine as a rapid-acting antidepressant and the development and refinement of tools capable of selectively altering the activity of populations of neuronal subtypes."5.05Prefrontal cortex circuits in depression and anxiety: contribution of discrete neuronal populations and target regions. ( Duman, RS; Hare, BD, 2020)
" ketamine; deep brain stimulation) that are reported to be effective in treatment-resistant depression and (iv) a parallel to a known clinical risk factor."4.91Treatment-resistant depression: are animal models of depression fit for purpose? ( Belzung, C; Willner, P, 2015)
"Ketamine intravenous therapy (KIT) appears effective for treating depression in controlled trials testing a short series of infusions."4.31The effects of ketamine on symptoms of depression and anxiety in real-world care settings: A retrospective controlled analysis. ( Heifets, BD; Hietamies, TM; Klise, AJ; Levine, SP; McInnes, LA; Qian, JJ; Williams, LM; Worley, MJ, 2023)
"Considering the increasing usage of ketamine as a recreational drug with hallucinogenic properties and also scarce studies about receptor systems responsible for its effects, in the present study we aimed to investigate whether the activation of the ventral hippocampal (VH) CB1 cannabinoid receptors affects the anxiety-like behaviors induced by ketamine."4.31Activation of ventral hippocampal CB1 receptors inhibits ketamine-induced anxiogenic-like behavior: Alteration of BDNF/c-Fos levels in the mouse hippocampus. ( Alijanpour, S; Rezayof, A, 2023)
"Ketamine is an anesthetic drug that has recently been approved for the treatment of treatment-resistant depression."4.31The Effects of Acute and Repeated Administration of Ketamine on Memory, Behavior, and Plasma Corticosterone Levels in Female Mice. ( Acevedo, J; Johnson, EM; Mugarura, NE; Siegel, JA; Welter, AL, 2023)
"Ketamine enhances the resilience against stress-induced depressive-like behavior, but its prophylactic efficacy in anxiety-related behaviors remains to be elucidated."4.12Prophylactic efficacy of ketamine, but not the low-trapping NMDA receptor antagonist AZD6765, against stress-induced maladaptive behavior and 4E-BP1-related synaptic protein synthesis impairment. ( Alves, EC; Camargo, A; Dalmagro, AP; Fraga, DB; Kouba, BR; Rodrigues, ALS; Torrá, ACNC; Valverde, AP, 2022)
"One hundred thirty-five Chinese individuals with anxious depression (n = 92) and nonanxious depression (n = 43) received six intravenous infusions of ketamine (0."4.12Antianhedonic effects of serial intravenous subanaesthetic ketamine in anxious versus nonanxious depression. ( Gu, LM; Ning, YP; Tan, JQ; Wang, CY; Yang, XH; Zheng, W; Zhou, YL, 2022)
"Ketamine has emerged as a promising pharmacotherapy for depression and other mental illnesses, and the intramuscular (IM) administration of ketamine is now offered at many North American outpatient psychiatric clinics."4.12Real-world depression, anxiety and safety outcomes of intramuscular ketamine treatment: a retrospective descriptive cohort study. ( Ahuja, S; Brendle, M; Moore, C; Robison, R; Smart, L; Thielking, P, 2022)
"The aim of this study was to examine the effect on depressive symptoms of repeated subanesthetic doses of SC esketamine in unipolar and bipolar treatment-resistant depression (TRD) and clinical predictors of response."4.02Repeated subcutaneous esketamine for treatment-resistant depression: Impact of the degree of treatment resistance and anxiety comorbidity. ( Abdo, G; B Andreoli, S; B Puertas, C; Barbosa, M; Cohrs, FM; Del Porto, JA; Del Sant, LC; Delfino, R; Fava, VA; Lacerda, AL; Liberatori, A; Lucchese, AC; Magalhães, EJM; Nakahira, C; Sarin, LM; Steiglich, MS; Surjan, J; Tuena, MA, 2021)
" The treatments with ketamine, guanosine, and ketamine plus guanosine were effective to counteract corticosterone-induced anxiety-like phenotype, but not disturbances in the hippocampal NLRP3 pathway."4.02Low doses of ketamine and guanosine abrogate corticosterone-induced anxiety-related behavior, but not disturbances in the hippocampal NLRP3 inflammasome pathway. ( Camargo, A; Dalmagro, AP; Fraga, DB; Kaster, MP; Rodrigues, ALS; Rosa, JM; Zeni, ALB, 2021)
" Ketamine is a unique and safe drug that enables well-controlled sedation and anesthesia, attenuates depression and mitigates suicidal thoughts, without depressing respiratory or cardiovascular mechanics."4.02Perspectives of Ketamine Use in COVID-19 Patients. ( Weinbroum, AA, 2021)
"Patients with TRD and prominent anxiety receiving IV ketamine exhibited a significant reduction in depressive, SI and anxiety symptoms."4.02The effectiveness of intravenous ketamine in adults with treatment-resistant major depressive disorder and bipolar disorder presenting with prominent anxiety: Results from the Canadian Rapid Treatment Center of Excellence. ( Gill, H; Ho, R; Kratiuk, K; Lee, Y; Lipsitz, O; Lui, LM; Mansur, RB; McIntyre, RS; Nasri, F; Rodrigues, NB; Rosenblat, JD; Subramaniapillai, M; Teopiz, K, 2021)
"Ketamine has rapid anxiolytic effects in treatment-resistant obsessive compulsive, post-traumatic stress, generalised anxiety and social anxiety disorders."4.02Anxiolytic effects of acute and maintenance ketamine, as assessed by the Fear Questionnaire subscales and the Spielberger State Anxiety Rating Scale. ( Glue, P; Gray, A; Neehoff, S; Nehoff, H; Truppman Lattie, D, 2021)
" Levels of the three markers did not correlate with ketamine use variables, craving, depression, or anxiety symptoms."3.96Chronic ketamine abuse is associated with orexin-A reduction and ACTH elevation. ( Chang, HM; Chen, CH; Chen, CK; Chen, LY; Huang, MC; Lin, SK; Xu, K, 2020)
"We included 104 patients with KD (76 males and 28 females) who received inpatient treatment for ketamine withdrawal and assessed them by using Beck Depression Inventory (BDI), Beck Anxiety Inventory, and a visual analog scale (VAS; 0-100 mm) for ketamine craving on day 2 to 3 of admission."3.96Association of Craving and Depressive Symptoms in Ketamine-Dependent Patients Undergoing Withdrawal Treatment. ( Chang, HM; Chen, CH; Chen, CK; Chen, LY; Huang, MC; Xu, K, 2020)
"Comparison of the S-ketamine group (n = 8; 4 male, 4 female; average age 52 years) with the control group (n = 8; 3 male, 5 female; average age 55 years) revealed a significant multivariate effect on anxiety and depression F(1, 14) = 4."3.96A rapid positive influence of S-ketamine on the anxiety of patients in palliative care: a retrospective pilot study. ( Cordes, J; Falk, E; Grau, I; Kienbaum, P; Lutterbeck, MJ; Neukirchen, M; Schlieper, D; Schwartz, J; van Caster, P, 2020)
"Here we show that mice prenatally exposed to ketamine displayed anxiety-like behaviors during adulthood, but not during puberty."3.96Prenatal Exposure to Ketamine Leads to Anxiety-Like Behaviors and Dysfunction in Bed Nucleus of Stria Terminalis. ( Chen, Y; Feng, X; Guo, H; Hu, Y; Li, Y; Lin, J; Lin, L; Liu, T; Lu, Z; Sun, J; Xu, S, 2020)
"To determine the effectiveness of intravenous (IV) ketamine on anxiety, irritability, agitation, and suicidality, in adults with treatment-resistant major depressive disorder (MDD) or bipolar disorder (BD)."3.96The effectiveness of ketamine on anxiety, irritability, and agitation: Implications for treating mixed features in adults with major depressive or bipolar disorder. ( Cha, DS; Fagiolini, A; Gill, H; Ho, R; Kratiuk, K; Lee, Y; Lin, K; Lipsitz, O; Malhi, GS; Mansur, RB; McIntyre, RS; Nasri, F; Rodrigues, NB; Rosenblat, JD; Subramaniapillai, M; Suppes, T; Vinberg, M, 2020)
"Arc-CreERT2 × CAG-Sun1/sfGFP mice showed sex differences in social and anxiety behavior and a different pattern between ketamine and (2R,6R)-HNK in the FST in male and female mice."3.96Sexually Dimorphic Behavioral Profile in a Transgenic Model Enabling Targeted Recombination in Active Neurons in Response to Ketamine and (2R,6R)-Hydroxynorketamine Administration. ( Herzog, DP; Lutz, B; Mellema, RM; Müller, MB; Remmers, F; Treccani, G, 2020)
" These behavioral effects are associated with i/ a reversal of anxiety and reduced self-care, ii/ a decrease in parenchymal cytokine production, iii/ a modulation of the microglial reactivity and iv/ a decrease in microglial quinolinic acid production that is correlated with plasmatic peripheral production."3.91Microglial production of quinolinic acid as a target and a biomarker of the antidepressant effect of ketamine. ( Abdel-Ahad, P; Blatzer, M; Callebert, J; Chrétien, F; Danckaert, A; de Maricourt, P; De Medeiros, GF; Gaillard, R; Jouvion, G; Langeron, O; Launay, JM; Maignan, A; Petit, AC; Sharshar, T; Van Steenwinckel, J; Verdonk, F; Vinckier, F, 2019)
"In this longitudinal study, 114 ketamine users completed clinical and cognitive assessments at both baseline and 12-week follow-up with the following instruments: Severity of Dependence Scale, Beck Depression Inventory (BDI), Anxiety Subscale of the Hospital Anxiety Depression Scale (HADSA), and a cognitive battery."3.91Recovery of cognitive functioning following abstinence from ketamine. ( Lane, HY; Lau, CG; Lin, SK; Tang, WK; Ungvari, GS, 2019)
"Patients with IBS who underwent elective colonoscopy procedures expressed higher pre-procedural anxiety scores, required more propofol consumption, and experienced more disruptive movements compared with controls."3.88Ambulatory colonoscopy under sedoanalgesia in adult patients with and without irritable bowel syndrome: A prospective, cross-sectional, and double-blind comparison. ( Araz, C; Çelebi, A; Tuncalı, B, 2018)
"This study tested the effects of ketamine on vulnerability of female adolescent mice to activity-based anorexia (ABA)."3.88Single injection of ketamine during mid-adolescence promotes long-lasting resilience to activity-based anorexia of female mice by increasing food intake and attenuating hyperactivity as well as anxiety-like behavior. ( Aoki, C; Chen, YW; Sherpa, AD, 2018)
"Ketamine may achieve its effects on treatment-resistant generalized anxiety disorder and social anxiety disorder through related mechanisms to the common reduction by conventional anxiolytic drugs in right frontal theta."3.88Ketamine Effects on EEG during Therapy of Treatment-Resistant Generalized Anxiety and Social Anxiety. ( Glue, P; Kawe, T; Martin, D; McNaughton, N; Neehoff, S; Shadli, SM, 2018)
"This study aimed to test stage- and dose-dependent effects of ketamine exposure on certain brain functions by evaluating alterations in locomotion, anxiety-like and avoidance behaviors, as well as socialization."3.85Behavioral alterations of zebrafish larvae after early embryonic exposure to ketamine. ( Antunes, LM; Coimbra, AM; Félix, LM; Valentim, AM, 2017)
"We report a case series on the observed effects of low-dose ketamine infusions in 4 critically ill patients with varying complications related to prolonged critical illness."3.83Low-Dose Ketamine in Chronic Critical Illness. ( Darrah, D; Moitra, A; Moitra, VK; Patel, MK; Wunsch, H, 2016)
"One of the most striking discoveries in the treatment of major depression was the finding that infusion of a single sub-anesthetic dose of ketamine induces rapid and sustained antidepressant effects in treatment-resistant depressed patients."3.83Repeated ketamine treatment induces sex-specific behavioral and neurochemical effects in mice. ( Mauch, J; Pandit, R; Pitychoutis, PM; Sens, J; Thelen, C, 2016)
"Ketamine (20 mg/kg) reversed the chronic unpredictable stress-induced depression-like behaviors in the FST."3.79Repeated ketamine exposure induces an enduring resilient phenotype in adolescent and adult rats. ( Alcantara, LF; Bolaños-Guzmán, CA; Hadad, R; Iñiguez, SD; Kroeck, KG; Parise, EM; Sial, OK; Warren, BL; Wright, KN, 2013)
" Here, two cases are reported in which a single oral dose of ketamine provided rapid and moderately sustained symptom relief for both depression and anxiety."3.76Oral ketamine for the rapid treatment of depression and anxiety in patients receiving hospice care. ( Iglewicz, A; Irwin, SA, 2010)
"It was investigated whether subchronic application of 30 mg/kg ketamine (Ket) induces reliable changes in behaviour and parameters of dopaminergic, glutamatergic, and serotonergic neurotransmissions, which might be the basis of an animal model in schizophrenia research."3.72Ketamine-induced changes in rat behaviour: A possible animal model of schizophrenia. ( Becker, A; Grecksch, G; Huether, G; Mann, T; Peters, B; Schroeder, H, 2003)
" Demographics, adverse events, and patient-reported dissociation were also analyzed."3.11At-home, sublingual ketamine telehealth is a safe and effective treatment for moderate to severe anxiety and depression: Findings from a large, prospective, open-label effectiveness trial. ( Akiki, TJ; Arden, K; Gazzaley, A; Hull, TD; Klotz, M; Madan, A; Malgaroli, M; Paleos, C; Swain, J; Vando, L, 2022)
"About 20 to 30 percent of patients with Major Depressive Disorder (MDD) do not respond to standard treatment and are considered treatment-resistant."2.90Anxiety during ketamine infusions is associated with negative treatment responses in major depressive disorder. ( Aust, S; Bajbouj, M; Basso, L; Chae, WR; Cosma, NC; Gärtner, M; Grimm, S; Heuser-Collier, I; Otte, C; Regen, F; van Hall, F; Wingenfeld, K, 2019)
"Ketamine is a noncompetitive antagonist of the N-methyl-d-aspartate (NMDA) glutamate receptor, which underlies its induction of pain relief and anaesthesia."2.82Ketamine treatment for refractory anxiety: A systematic review. ( Brooks, S; Dahlén, AD; Haggarty, CJ; Schiöth, HB; Tully, JL, 2022)
"The incidence of postoperative pain and vomiting as well as the severity of postoperative pain were compared between study groups during the 6-hour postoperative period using a visual analog scale (VAS) at rest, upon swallowing saliva, drinking liquids and eating ice cream."2.76Intravenous and peritonsillar infiltration of ketamine for postoperative pain after adenotonsillectomy: a randomized placebo-controlled clinical trial. ( Dehghankhalili, M; Ghaffarpasand, F; Heiran, HR; Khademi, S; Motazedian, S; Yavari, MJ, 2011)
"Patients with major depressive disorder often have limited response to first-line and second-line medications; hence, novel pharmacological treatments are needed for treatment-resistant depression (TRD)."2.72The Canadian Network for Mood and Anxiety Treatments (CANMAT) Task Force Recommendations for the Use of Racemic Ketamine in Adults with Major Depressive Disorder: Recommandations Du Groupe De Travail Du Réseau Canadien Pour Les Traitements De L'humeur Et ( Beaulieu, S; Blier, J; Blier, P; Brietzke, E; Frey, BN; Kennedy, SH; Lam, RW; McGirr, A; McIntyre, RS; Milev, RV; Parikh, SV; Ravindran, AV; Ravindran, N; Richard-Devantoy, S; Schaffer, A; Swainson, J; Taylor, VH; Tourjman, V; van Ameringen, M; Yatham, LN, 2021)
" The most common treatment-emergent adverse events associated with ketamine/esketamine are dissociation, anxiety, nausea, increased blood pressure, and headache."2.72Prevention and Management of Common Adverse Effects of Ketamine and Esketamine in Patients with Mood Disorders. ( Cao, B; Ceban, F; Chau, EH; Gill, H; Ho, RC; Kratiuk, K; Kumar, A; Lee, JG; Lee, Y; Lin, K; Lipsitz, O; Lui, LMW; Mansur, RB; McIntyre, RS; Nasri, F; Rodrigues, NB; Rosenblat, JD; Subramaniapillai, M; Swainson, J, 2021)
"Nimodipine pretreatment attenuated the perceived similarity of ketamine effects to ethanol as well as ketamine-induced euphoria and sedation."2.70Attenuation of ketamine effects by nimodipine pretreatment in recovering ethanol dependent men: psychopharmacologic implications of the interaction of NMDA and L-type calcium channel antagonists. ( Burakov, AM; Fletcher, J; Grinenko, AY; Grinenko, NI; Krupitsky, EM; Krystal, JH; Petrakis, IL; Romanova, TN, 2001)
"001) but times from dosing to discharge (medians 105 and 110 minutes) were similar."2.70Sedation for children requiring wound repair: a randomised controlled double blind comparison of oral midazolam and oral ketamine. ( Kendall, JM; Younge, PA, 2001)
" The control group and the test groups were comparable with regard to biological data, duration of operation, applied dosage of local anaesthetics and actual anxiety before operation."2.68[Analgesia-sedation for maxillo-facial surgery with midazolam-pentazocine and miazolam-ketamine. Clinical double-blind study of anxiety, analgesia, sedation and amnesia]. ( Daubländer, M; Dick, W; Lipp, M; Sebastian, M, 1995)
" The use of MAD even gives as better bioavailability of drugs."2.58Intranasal drug administration for procedural sedation in children admitted to pediatric Emergency Room. ( Chiaretti, A; Fabrizio, GC; Fantacci, C; Ferrara, P; Franceschi, F, 2018)
" It also reviews the comparative pharmacokinetics, adverse effects, and dosing of ketamine, propofol, and ketofol as agents for procedural sedation and analgesia."2.48Ketamine, propofol, and ketofol use for pediatric sedation. ( Alletag, MJ; Auerbach, MA; Baum, CR, 2012)
"Ketamine, which acts as a noncompetitive antagonist of glutamatergic NMDA receptors by binding to the phencyclidine site, may induce schizophrenia-like symptoms and promote anxiogenic-like behaviour."1.51Comparison of the effects of 1MeTIQ and olanzapine on performance in the elevated plus maze test and monoamine metabolism in the brain after ketamine treatment. ( Antkiewicz-Michaluk, L; Białoń, M; Wąsik, A; Żarnowska, M, 2019)
"Ketamine has become increasingly popular in adolescent drug abusers worldwide."1.51The effects of sub-anesthetic ketamine plus ethanol on behaviors and apoptosis in the prefrontal cortex and hippocampus of adolescent rats. ( Fan, SJ; Jiang, H; Li, Q; Liu, DX; Pan, F; Wu, HR; Zhang, Q, 2019)
" The higher ketamine use frequency and dosage were associated with more severe depressive symptoms."1.43Profiling the psychotic, depressive and anxiety symptoms in chronic ketamine users. ( Deng, X; Ding, Y; Fan, N; He, H; Ke, X; Ning, Y; Rosenheck, R; Sun, B; Tang, W; Wang, D; Xu, K; Zhou, C, 2016)
"Ketamine (Ketalar®) is a non-competitive glutamatergic antagonist classically used to induce sedation."1.42Behavioral, endocrine, and neuronal alterations in zebrafish (Danio rerio) following sub-chronic coadministration of fluoxetine and ketamine. ( Hylton, A; Pittman, J, 2015)
"Ketamine is an anesthetic with antidepressant properties."1.42The positive effect on ketamine as a priming adjuvant in antidepressant treatment. ( Dalla, C; Ferreira, C; Kokras, N; Melo, A; Pêgo, JM; Sousa, N; Ventura-Silva, AP, 2015)
"Ketamine users are often poly-substance users."1.39Cognitive impairments in poly-drug ketamine users. ( Chan, F; Lau, CG; Liang, HJ; Tang, A; Tang, WK; Ungvari, GS, 2013)
"Ketamine is a non-competitive N-methyl-D-aspartate receptor antagonist that is Food and Drug Administration-approved in the United States for anesthesia due to its sedative effects with low risk of severe respiratory depression."1.39Two cases of delayed-onset suicidal ideation, dysphoria and anxiety after ketamine infusion in patients with obsessive-compulsive disorder and a history of major depressive disorder. ( Bloch, MH; Corlett, PR; Grunschel, BD; Niciu, MJ; Pittenger, C, 2013)
"Ketamine post-SE onset treatment prevented neuronal death in all regions assessed."1.38Ketamine reduces neuronal degeneration and anxiety levels when administered during early life-induced status epilepticus in rats. ( Córdova, SD; de Oliveira, DL; Loss, CM, 2012)
"Tachycardia was the most common physical examination finding."1.31Ketamine abusers presenting to the emergency department: a case series. ( Bayer, MJ; McKay, CA; Vieira, L; Weiner, AL, 2000)
"The ketamine group was superior to the conventional group which was superior to the no-treatment group in reducing negative affect experienced during stressful situations."1.26Ketamine-facilitated induced anxiety therapy and its effect upon clients' reactions to stressful situations. ( Becker, AT; Corssen, G; Sappington, AA; Tavakoli, M, 1979)
"Fifty-six young and 29 middle-aged adults who were scheduled for lower abdominal, anorectal or extremity surgery under epidural, sacral or brachial plexus blockades received intravenous analgesic or anaesthetic doses of ketamine, combined with diazepam, immediately before the start of the operation."1.26Untoward effects of ketamine combined with diazepam for supplementing conduction anaesthesia in young and middle-aged adults. ( Korttila, K; Levänen, J, 1978)

Research

Studies (138)

TimeframeStudies, this research(%)All Research%
pre-199013 (9.42)18.7374
1990's5 (3.62)18.2507
2000's16 (11.59)29.6817
2010's60 (43.48)24.3611
2020's44 (31.88)2.80

Authors

AuthorsStudies
Camargo, A2
Torrá, ACNC1
Dalmagro, AP2
Valverde, AP1
Kouba, BR1
Fraga, DB3
Alves, EC1
Rodrigues, ALS3
Michelotti, P1
Franscescon, F1
Müller, TE1
Rosemberg, DB1
Pereira, ME1
Zoladz, PR1
Del Valle, CR1
Goodman, CS1
Dodson, JL1
Smith, IF1
Elmouhawesse, KM1
Sparkman, HR1
Naylor, MM1
Hopson, EP1
Tully, JL1
Dahlén, AD1
Haggarty, CJ1
Schiöth, HB1
Brooks, S1
Zheng, W2
Yang, XH1
Gu, LM1
Tan, JQ1
Zhou, YL1
Wang, CY1
Ning, YP1
Hull, TD1
Malgaroli, M1
Gazzaley, A1
Akiki, TJ1
Madan, A1
Vando, L1
Arden, K1
Swain, J1
Klotz, M1
Paleos, C1
Acevedo, J3
Siegel, JA3
Pałucha-Poniewiera, A1
Oliver, PA1
Snyder, AD1
Feinn, R1
Malov, S1
McDiarmid, G1
Arias, AJ1
Ahuja, S1
Brendle, M1
Smart, L1
Moore, C1
Thielking, P1
Robison, R1
Mugarura, NE2
Welter, AL2
Johnson, EM2
Pastuszak, M1
Wiglusz, MS1
da Silveira, CCM1
Cartágenes, SC1
Kobayashi, NHC1
Farias, SV1
de Souza-Junior, FJC1
Fernandes, LMP1
do Prado, AF1
Aragão, WAB1
Lima, RR1
Ferreira, WAS1
de Oliveira, EHC1
Mello Júnior, FAR1
Burbano, RMR1
Fontes-Júnior, EA1
Maia, CDSF1
Alijanpour, S1
Rezayof, A1
Subramanian, S1
Oughli, HA1
Gebara, MA1
Palanca, BJA1
Lenze, EJ1
Hietamies, TM1
McInnes, LA1
Klise, AJ1
Worley, MJ1
Qian, JJ1
Williams, LM1
Heifets, BD1
Levine, SP1
Bartsch, CJ1
Aaflaq, S1
Jacobs, JT1
Smith, M1
Summa, F1
Skinner, S1
Qasem, E1
Thompson, R1
Li, Z1
Nordman, JC1
Chen, Y2
Yan, P1
Wei, S1
Zhu, Y1
Lai, J1
Zhou, Q1
Curpan, AS1
Savuca, A1
Hritcu, LD1
Solcan, C1
Nicoara, MN1
Luca, AC1
Ciobica, AS1
Liu, W1
Zhou, Y1
Wang, C2
Zhan, Y1
Lan, X1
Zhang, B1
Li, H1
Chen, L1
Ning, Y2
Wang, W2
Zhou, T1
Jia, R1
Zhang, H2
Zhang, Y1
Dong, Y1
Wang, J2
Sheng, L1
Wu, H1
Chen, G1
Xue, W1
Tang, WK2
Lau, CG2
Ungvari, GS2
Lin, SK2
Lane, HY1
Chen, LY2
Chen, CK2
Chen, CH2
Chang, HM2
Huang, MC2
Xu, K3
Wu, C1
Wang, Y2
He, Y1
Wu, S1
Xie, Z2
Zhang, J1
Shen, J1
Wang, Z1
He, L1
Falk, E1
Schlieper, D1
van Caster, P1
Lutterbeck, MJ1
Schwartz, J1
Cordes, J1
Grau, I1
Kienbaum, P1
Neukirchen, M1
Silote, GP1
de Oliveira, SFS1
Ribeiro, DE1
Machado, MS1
Andreatini, R1
Joca, SRL1
Beijamini, V1
Sun, J1
Lin, J1
Feng, X1
Lu, Z1
Liu, T1
Lin, L1
Hu, Y1
Li, Y1
Xu, S1
Guo, H1
Hare, BD1
Duman, RS1
Kamel, AAF1
Amin, OAI1
Herzog, DP1
Mellema, RM1
Remmers, F1
Lutz, B1
Müller, MB1
Treccani, G1
McIntyre, RS4
Lipsitz, O3
Rodrigues, NB3
Lee, Y3
Cha, DS1
Vinberg, M1
Lin, K2
Malhi, GS1
Subramaniapillai, M3
Kratiuk, K3
Fagiolini, A1
Gill, H3
Nasri, F3
Mansur, RB3
Suppes, T1
Ho, R2
Rosenblat, JD3
Chen, MH2
Lin, WC2
Wu, HJ2
Bai, YM2
Li, CT2
Tsai, SJ2
Hong, CJ2
Tu, PC2
Cheng, CM2
Su, TP2
Truppman Lattie, D1
Nehoff, H1
Neehoff, S4
Gray, A3
Glue, P4
Zhang, X1
Kong, Y1
He, G1
Zhou, Z1
Lamanna, J1
Isotti, F1
Ferro, M1
Racchetti, G1
Anchora, L1
Rucco, D1
Malgaroli, A1
Munkholm, K1
Jørgensen, KJ1
Lui, LM1
Teopiz, K1
Swainson, J2
McGirr, A1
Blier, P1
Brietzke, E1
Richard-Devantoy, S1
Ravindran, N1
Blier, J1
Beaulieu, S1
Frey, BN1
Kennedy, SH1
Milev, RV1
Parikh, SV1
Schaffer, A1
Taylor, VH1
Tourjman, V1
van Ameringen, M1
Yatham, LN1
Ravindran, AV1
Lam, RW1
Lucchese, AC1
Sarin, LM1
Magalhães, EJM1
Del Sant, LC1
B Puertas, C1
Tuena, MA1
Nakahira, C1
Fava, VA1
Delfino, R1
Surjan, J1
Steiglich, MS1
Barbosa, M1
Abdo, G1
Cohrs, FM1
Liberatori, A1
Del Porto, JA1
Lacerda, AL1
B Andreoli, S1
Weinbroum, AA1
Reddy, BR1
Babu, NS1
Das, T1
Bhattacharya, D1
Murthy, CLN1
Kumar, A2
Idris, MM1
Chakravarty, S1
Zarate, CA2
Daly, EJ1
Turkoz, I1
Salvadore, G1
Fedgchin, M1
Ionescu, DF3
Starr, HL1
Borentain, S1
Trivedi, MH2
Thase, ME1
Singh, JB1
Rosa, JM1
Zeni, ALB1
Kaster, MP1
Ceban, F1
Lui, LMW1
Lee, JG1
Chau, EH1
Cao, B1
Ho, RC1
Medlicott, NJ1
Harland, S1
Anderson-Fahey, B1
Le Nedelec, M1
McNaughton, N2
Canpolat, DG1
Yildirim, MD1
Kutuk, N1
Dogruel, F1
Ocak, H1
Aksu, R1
Alkan, A1
Onaolapo, OJ1
Paul, TB1
Onaolapo, AY1
Castle, C1
Pearce, JI1
Brousseau, DC1
Yan, K1
Hainsworth, KR1
Hoffmann, RG1
Drendel, AL1
Qiao, H1
Jia, J1
Guarraci, FA1
Gonzalez, CMF1
Lucero, D1
Womble, PD1
Abdel-Rahim, H1
DeVore, J1
Kunkel, MN1
Quadlander, E1
Stinnett, M1
Boyette-Davis, J1
Fantacci, C1
Fabrizio, GC1
Ferrara, P1
Franceschi, F1
Chiaretti, A2
Olescowicz, G1
Moretti, M1
Siteneski, A1
Tavares, MK1
Azevedo, D1
Colla, ARS1
Fallon, MT2
Wilcock, A1
Kelly, CA1
Paul, J1
Lewsley, LA1
Norrie, J1
Laird, BJA1
Shadli, SM1
Kawe, T1
Martin, D1
Tuncalı, B1
Araz, C1
Çelebi, A1
Aguilar-Valles, A1
Haji, N1
De Gregorio, D1
Matta-Camacho, E1
Eslamizade, MJ1
Popic, J1
Sharma, V1
Cao, R1
Rummel, C1
Tanti, A1
Wiebe, S1
Nuñez, N1
Comai, S1
Nadon, R1
Luheshi, G1
Mechawar, N1
Turecki, G2
Lacaille, JC1
Gobbi, G1
Sonenberg, N1
Chen, YW1
Sherpa, AD1
Aoki, C1
Salloum, NC1
Fava, M1
Freeman, MP1
Flynn, M1
Hoeppner, B1
Hock, RS1
Cusin, C1
Iosifescu, DV1
Sanacora, G1
Mathew, SJ1
Debattista, C1
Papakostas, GI1
Akhlaghi, N1
Payandemehr, P1
Yaseri, M1
Akhlaghi, AA1
Abdolrazaghnejad, A1
Pitsikas, N2
Georgiadou, G1
Delis, F1
Antoniou, K1
Liu, L1
Yang, X1
Gao, H1
Tang, QK1
Yin, LY1
Yin, XY1
Hao, JR1
Geng, DQ1
Gao, C1
Aust, S1
Gärtner, M1
Basso, L1
Otte, C1
Wingenfeld, K1
Chae, WR1
Heuser-Collier, I1
Regen, F1
Cosma, NC1
van Hall, F1
Grimm, S1
Bajbouj, M1
Wąsik, A1
Białoń, M1
Żarnowska, M1
Antkiewicz-Michaluk, L1
Schatzberg, AF2
Verdonk, F1
Petit, AC1
Abdel-Ahad, P1
Vinckier, F1
Jouvion, G1
de Maricourt, P1
De Medeiros, GF1
Danckaert, A1
Van Steenwinckel, J1
Blatzer, M1
Maignan, A1
Langeron, O1
Sharshar, T1
Callebert, J1
Launay, JM1
Chrétien, F1
Gaillard, R1
Ren, W1
Liu, X2
Cheng, L1
Wang, G1
Peng, L1
Li, Q1
Wu, HR1
Fan, SJ1
Liu, DX1
Jiang, H1
Zhang, Q1
Pan, F1
Chaki, S1
Niciu, MJ2
Grunschel, BD1
Corlett, PR1
Pittenger, C1
Bloch, MH1
Parise, EM1
Alcantara, LF1
Warren, BL1
Wright, KN1
Hadad, R1
Sial, OK1
Kroeck, KG1
Iñiguez, SD1
Bolaños-Guzmán, CA1
Liang, HJ1
Tang, A1
Chan, F1
Sufka, KJ1
White, SW1
Blednov, YA1
Benavidez, JM1
Black, M1
Leiter, CR1
Osterndorff-Kahanek, E1
Johnson, D1
Borghese, CM1
Hanrahan, JR1
Johnston, GA1
Chebib, M1
Harris, RA1
Kilic, FS1
Ismailoglu, S1
Kaygisiz, B1
Oner, S1
Luckenbaugh, DA1
Richards, EM1
Raud, S1
Reimets, R1
Loomets, M1
Sütt, S1
Altpere, A1
Visnapuu, T1
Innos, J1
Luuk, H1
Plaas, M1
Volke, V1
Vasar, E1
Moitra, VK1
Patel, MK1
Darrah, D1
Moitra, A1
Wunsch, H1
Brachman, RA1
McGowan, JC1
Perusini, JN1
Lim, SC1
Pham, TH1
Faye, C1
Gardier, AM1
Mendez-David, I1
David, DJ1
Hen, R1
Denny, CA1
Melo, A1
Kokras, N1
Dalla, C1
Ferreira, C1
Ventura-Silva, AP1
Sousa, N1
Pêgo, JM1
De Campos, EG1
Bruni, AT1
De Martinis, BS1
Sobota, R1
Mihara, T1
Forrest, A1
Featherstone, RE1
Siegel, SJ1
Willner, P1
Belzung, C1
Pittman, J1
Hylton, A1
Bolton, JM1
Gunnell, D1
Reardon, S1
Trevlopoulou, A1
Touzlatzi, N1
Fan, N1
Rosenheck, R1
Wang, D1
Ke, X1
Ding, Y1
Sun, B1
Zhou, C1
Deng, X1
Tang, W1
He, H1
Holubova, K1
Kleteckova, L1
Skurlova, M1
Ricny, J1
Stuchlik, A1
Vales, K1
Thelen, C1
Sens, J1
Mauch, J1
Pandit, R1
Pitychoutis, PM1
Sun, XR1
Zhang, ZZ1
Zhao, HT1
Li, HH1
Ji, MH1
Li, KY1
Yang, JJ1
Félix, LM1
Antunes, LM1
Coimbra, AM1
Valentim, AM1
Engin, E1
Treit, D1
Dickson, CT1
Ruggiero, A1
Barone, G1
Antonelli, A1
Lazzareschi, I1
Genovese, O1
Paiano, S1
Sammartino, M1
Maurizi, P1
Riccardi, R1
Jain, K1
Ghai, B1
Saxena, AK1
Saini, D1
Khandelwal, N1
Irwin, SA1
Iglewicz, A1
Khademi, S1
Ghaffarpasand, F1
Heiran, HR1
Yavari, MJ1
Motazedian, S1
Dehghankhalili, M1
Darlong, V1
Shende, D1
Singh, M1
Garg, R1
Pandey, R1
Punj, J1
Hosseini Jahromi, SA1
Hosseini Valami, SM1
Adeli, N1
Yazdi, Z1
Loss, CM1
Córdova, SD1
de Oliveira, DL1
Alletag, MJ1
Auerbach, MA1
Baum, CR1
Krupitsky, E1
Burakov, A1
Romanova, T1
Dunaevsky, I1
Strassman, R1
Grinenko, A1
Silvestre, JS1
Pallarés, M1
Nadal, R1
Ferré, N1
Shi, L1
Fatemi, SH1
Sidwell, RW1
Patterson, PH1
Becker, A1
Peters, B1
Schroeder, H1
Mann, T1
Huether, G1
Grecksch, G1
Hayase, T1
Yamamoto, Y1
Yamamoto, K1
Pavarin, RM1
Ryhänen, P1
Kangas, T1
Rantakylä, S1
Warner, DL1
Cabaret, J1
Velling, D1
Lipp, M1
Daubländer, M1
Sebastian, M1
Dick, W2
Kennedy, RM2
Porter, FL1
Miller, JP1
Jaffe, DM1
Carpenter, WT1
Sherwin, TS1
Green, SM2
Khan, A1
Chapman, DS1
Dannenberg, B1
McAllister, JD1
Weiner, AL1
Vieira, L1
McKay, CA1
Bayer, MJ1
Oda, A1
Iida, H1
Dohi, S1
Younge, PA1
Kendall, JM1
Krauss, B1
Babar, E1
Ozgünen, T1
Melik, E1
Polat, S1
Akman, H1
Krupitsky, EM1
Burakov, AM1
Romanova, TN1
Grinenko, NI1
Grinenko, AY1
Fletcher, J1
Petrakis, IL1
Krystal, JH1
Mitchell, AC1
Knoche, E1
Traub, E1
Sappington, AA2
Corssen, G2
Becker, AT2
Tavakoli, M2
Modvig, KM1
Nielsen, SF1
Korttila, K1
Levänen, J1
Kaplan, S1
Hirschowitz, AS1
Nakamura, R1
Johnson, NE1
Mendoza Mendoza, A1
Solano Reina, E1
Mogensen, JV1
Misfeldt, BB1
Hanel, HK1
Magbagbeola, JA1
Thomas, NA1
Garfield, JM1
Garfield, FB1
Stone, JG1
Hopkins, D1
Johns, LA1
Unni, VK1
Bovill, JG1
Crusius, HG1

Clinical Trials (20)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Randomized, Double-blind, Multicenter, Active-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Flexible Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Subjects With Treatment-resistant Depression[NCT02418585]Phase 3236 participants (Actual)Interventional2015-08-07Completed
Ketamine Infusion for Social Anxiety Disorder[NCT02083926]Early Phase 118 participants (Actual)Interventional2015-01-02Completed
Pediatric Procedural Sedation and the Relationship With Post-Discharge Negative Behavioral Changes in the Emergency Department[NCT03980067]201 participants (Actual)Interventional2019-05-17Completed
Intranasal Sufentanil for Analgesia of Severe Sickle Cell Vaso-occlusive Pain Crisis in the Pediatric Emergency Department: a Double Blind Randomized Versus Placebo Controlled Trial[NCT06181695]Phase 3182 participants (Anticipated)Interventional2024-05-02Not yet recruiting
Intranasal Dexmedetomidine and Fentanyl Versus Intravenous Midazolam and Ketamine in Sedation for Painful Outpatient Procedures[NCT04621110]Phase 360 participants (Anticipated)Interventional2021-06-01Not yet recruiting
A Pilot Study of the Use of Oral Ketamine for Treatment of Vaso-Occlusive Pain in Adolescents and Young Adults[NCT05378555]Phase 310 participants (Anticipated)Interventional2023-05-01Recruiting
A Comparison of Midazolam or Haloperidol Premedication Versus Placebo for Reducing Ketamine Induced Agitation After Adult Procedural Sedation in the Emergency Department[NCT02909465]Phase 4185 participants (Actual)Interventional2016-07-31Completed
Positive Imagery Therapy and the Incidence of Emergence Reactions With the Use of Ketamine[NCT04746079]180 participants (Anticipated)Interventional2021-02-05Recruiting
Phenomenological Explorations of the Esketamine-Induced Transient Dissociative State[NCT06133309]15 participants (Anticipated)Interventional2023-12-01Not yet recruiting
Prediction of the Therapeutic Response in Depression Based on an Early Neuro-computational Modeling Assessment of Motivation[NCT05866575]136 participants (Anticipated)Interventional2023-06-01Not yet recruiting
Ketamine Infusion for Obsessive-Compulsive Disorder[NCT01349231]Phase 210 participants (Actual)Interventional2009-02-28Completed
Investigation of the Rapid (Next Day) Antidepressant Effects of an NMDA Antagonist[NCT00088699]Phase 1/Phase 267 participants (Actual)Interventional2004-07-26Completed
The Effect of Therapeutic Ketamine Infusions on the Symptoms of Post-Traumatic Stress Disorder in Combat Veterans[NCT03088384]30 participants (Actual)Observational2016-11-28Completed
Ketofol Versus Fentofol for Procedural Sedation of Children 3 to 17 Years Old: a Double-Blind Randomized Controlled Trial[NCT02079090]Phase 330 participants (Actual)Interventional2014-07-31Completed
Conscious Dying/Conscious Living: Ketamine-Assisted Psychotherapy (KAP) for Patients at End of Life-A Pilot Study for Palliative and Hospice Care[NCT05214417]Phase 2120 participants (Anticipated)Interventional2022-05-01Not yet recruiting
Anxiolysis for Emergency Department Procedures in Pediatric Patients Using Intranasal Ketamine Compared With Intranasal Midazolam: A Randomized Controlled Trial[NCT03043430]Phase 410 participants (Actual)Interventional2016-05-31Terminated (stopped due to Research manpower shortage)
Ketamine Versus Etomidate for Procedural Sedation for Pediatric Orthopedic Reductions[NCT00596050]Phase 450 participants (Actual)Interventional2006-08-31Completed
Systemic Absorption of Lidocaine After Ultrasound Guided Hematoma Block for Reduction of Different Types of Pediatric Distal Radius Fractures[NCT04359017]Phase 40 participants (Actual)Interventional2020-11-01Withdrawn (stopped due to Sponsoring staff have left institution)
Midazolam Effect on Agitation Postnasal Surgery: A Double Blinded Randomized Controlled Trial[NCT05165914]100 participants (Actual)Interventional2021-05-27Completed
Initiating Ketamine in Acutely Suicidal Patients in the Emergency Department[NCT04260607]Phase 32 participants (Actual)Interventional2020-01-14Terminated (stopped due to As a busy MTF we were unable to retain a health care provider with the appropriate expertise to buy-in to this study once the initiating PI left military service.)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Change From Baseline in Clinical Global Impression-Severity (CGI-S) Total Score up to Endpoint (Double-blind Induction Phase [Day 28])

"CGI-S provides measure of severity of participant's illness including participant's history, psychosocial circumstances, symptoms, behavior and impact of symptoms on ability to function. CGI-S evaluates severity of psychopathology on scale of 0 to 7. Considering total clinical experience, participant is assessed on severity of mental illness according to: 0=not assessed; 1=normal (not at all ill); 2=borderline mentally ill; 3=mildly ill; 4=moderately ill; 5=markedly ill; 6=severely ill; 7=among most extremely ill patients. CGI-S permits global evaluation of participant's condition at given time. The last post baseline observation during the phase was carried forward as End Point for that phase." (NCT02418585)
Timeframe: Baseline up to Endpoint (Double-blind Induction Phase [Day 28])

InterventionUnits on a scale (Median)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-2.0
Intranasal Placebo Plus Oral AD-2.0

Change From Baseline in EQ 5D-5L- European Quality of Life - Visual Analogue Scale (EQ-VAS) to End of Double-blind Induction Phase (Day 28)

EQ-5D-5L is a 2-part instrument for use as a measure of health outcome, designed for self-completion by respondents. It consists of EQ-5D-5L descriptive system and EQ VAS. The EQ VAS self-rating records the respondent's own assessment of his or her overall health status at the time of completion, on a scale of 0 (the worst health you can imagine) to 100 (the best health you can imagine). (NCT02418585)
Timeframe: Baseline up to End of Double-blind Induction Phase (Day 28)

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)29.1
Intranasal Placebo Plus Oral AD20.9

Change From Baseline in EQ 5D-5L- Sum Score to End of Double-blind Induction Phase (Day 28)

"EQ-5D-5L consists of EQ-5D-5L descriptive system and EQ visual analogue scale (EQ VAS). EQ-5D-5L descriptive system comprises of 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each has 5 levels of perceived problems (1-no problem, 2-slight problems, 3-moderate problems, 4-severe problems, 5-extreme problems). Participant selects answer for each of 5 dimensions considering response that best matches his/her health today. Responses were used to generate a Health Status Index (HSI). Health Status Index range is -0.148 - 0.949, is anchored at 0 (dead) and 1 (full health). EQ VAS self-rating records the respondent's own assessment of his/her overall health status at time of completion, on a scale of 0 (worst health you can imagine) to 100 (best health you can imagine). Sum score ranges from 0 to 100 where, sum score = (sum of the scores from the 5 dimensions minus 5) *5. Higher score indicates worst health state." (NCT02418585)
Timeframe: Baseline up to End of Double-blind Induction Phase (Day 28)

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-23.2
Intranasal Placebo Plus Oral AD-17.1

Change From Baseline in EQ 5D-5L-Health Status Index to End of Double-blind Induction Phase (Day 28)

"European Quality of Life Group-5 Dimension-5-Level (EQ-5D-5L) is a 2-part instrument for use as a measure of health outcome, designed for self-completion by respondents. It consists of EQ-5D-5L descriptive system and EQ VAS. EQ-5D-5L descriptive system comprises of 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each has 5 levels of perceived problems (1-no problem, 2-slight problems, 3-moderate problems, 4-severe problems, 5-extreme problems). Participant selects answer for each of 5 dimensions considering response that best matches his/her health today. Responses were used to generate a Health Status Index (HSI). Health Status Index range is -0.148 - 0.949, is anchored at 0 (dead) and 1 (full health)." (NCT02418585)
Timeframe: Baseline up to End of Double-blind Induction Phase (Day 28)

InterventionUnits on a Scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)0.288
Intranasal Placebo Plus Oral AD0.231

Change From Baseline in Generalized Anxiety Disorder (GAD-7) Total Score up to Endpoint (Double-blind Induction Phase [Day 28])

"GAD-7 is a brief and validated 7-item self-report assessment of overall anxiety. Participants respond to each item using a 4-point scale with response categories of 0=not at all, 1=several days, 2=more than half the days, and 3=nearly every day. Item responses are summed to yield a total score with a range of 0 to 21, where higher scores indicate more anxiety. The recall period is 2 weeks. The severity of the GAD-7 is categorized as follows: None (0-4), Mild (5-9), Moderate (10-14) and Severe (15 -21). The last post baseline observation during the phase was carried forward as End Point for that phase." (NCT02418585)
Timeframe: Baseline up to Endpoint (Double-blind Induction Phase [Day 28])

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-7.9
Intranasal Placebo Plus Oral AD-6.8

Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Total Score up to Day 28 in the Double-blind Induction Phase- Mixed-Effects Model Using Repeated Measures (MMRM) Analysis

MADRS is clinician-rated scale designed to measure depression severity, and to detect changes due to antidepressant treatment. Scale consists of 10 items (apparent sadness, reported sadness, inner tension, sleep, appetite, concentration, lassitude, interest level, pessimistic thoughts, and suicidal thoughts), each of which is scored from 0 (item is not present or is normal) to 6 (severe or continuous presence of symptoms), summed for a total possible score of 0 to 60. Higher scores represent more severe condition. (NCT02418585)
Timeframe: Baseline up to Day 28 of Double-blind Induction Phase

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-21.4
Intranasal Placebo Plus Oral AD-17.0

Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Total Score up to Endpoint (Double-blind Induction Phase [Day 28])- Analysis of Covariance (ANCOVA) Analysis

"MADRS is clinician-rated scale designed to measure depression severity, and to detect changes due to antidepressant treatment. Scale consists of 10 items (apparent sadness, reported sadness, inner tension, sleep, appetite, concentration, lassitude, interest level, pessimistic thoughts, and suicidal thoughts), each of which is scored from 0 (item is not present or is normal) to 6 (severe or continuous presence of symptoms), summed for a total possible score of 0 to 60. Higher scores represent more severe condition. The last post baseline observation during the phase was carried forward as End Point for that phase." (NCT02418585)
Timeframe: Baseline up to Endpoint (Double-blind Induction Phase [Day 28])

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-19.6
Intranasal Placebo Plus Oral AD-16.3

Change From Baseline in Patient Health Questionnaire - 9-Item Depression Module (PHQ-9) Total Score up to Day 28 of Double-blind Induction Phase- MMRM Analysis

PHQ-9 is 9-item, self-report scale assessing depressive symptoms. Each item is rated on 4-point scale (0=Not at all, 1=Several Days, 2=More than half days, 3=Nearly every day. Scale scores each of 9 symptom domains of Diagnostic and Statistical Manual of Mental Disorders, Major Depressive Disorder criteria and it has been used both as screening tool and measure of response to treatment for depression. The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. Severity of PHQ-9 categorized as follows: None-minimal (0-4), Mild (5-9), Moderate (10-14), Moderately Severe (15-19), Severe (20-27). (NCT02418585)
Timeframe: Baseline up to Day 28 of Double-blind Induction phase

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-13.0
Intranasal Placebo Plus Oral AD-10.2

Change From Baseline in Patient Health Questionnaire - 9-Item Depression Module (PHQ-9) Total Score up to Endpoint (Double-blind Induction Phase [Day 28])- ANCOVA Analysis

"PHQ-9 is 9-item, self-report scale assessing depressive symptoms. Each item is rated on 4-point scale (0=Not at all, 1=Several Days, 2=More than half days, 3=Nearly every day). Scale scores each of 9 symptom domains of Diagnostic and Statistical Manual of Mental Disorders, Major Depressive Disorder criteria and it has been used both as screening tool and measure of response to treatment for depression. The participant's item responses are summed to provide a total score (range of 0 to 27) with higher scores indicating greater severity of depressive symptoms. Severity of PHQ-9 categorized as follows: None-minimal (0-4), Mild (5-9), Moderate (10-14), Moderately Severe (15-19), Severe (20-27). The last post baseline observation during the phase was carried forward as End Point for that phase." (NCT02418585)
Timeframe: Baseline up to Endpoint (Double-blind Induction Phase [Day 28])

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-12.2
Intranasal Placebo Plus Oral AD-10.1

Change From Baseline in Sheehan Disability Scale (SDS) Total Score up to Day 28 of Double-blind Induction Phase- MMRM Analysis

The SDS is a participant-reported outcome measure and 5 item questionnaire used for assessment of functional impairment and associated disability. First three items assess disruption of 1 work/school, 2 social life, 3 family life/home responsibilities using a 0(no impairment)-10 (most severe impairment). Score for first 3 items are summed to create total score of 0-30 where higher score indicates greater impairment and a negative change in score indicates improvement. It also has one item on days lost from school or work and one item on days when under productive. (NCT02418585)
Timeframe: Baseline up to Day 28 of Double-blind Induction phase

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-13.6
Intranasal Placebo Plus Oral AD-9.4

Change From Baseline in Sheehan Disability Scale (SDS) Total Score up to Endpoint (Double-blind Induction Phase [Day 28])- ANCOVA Analysis

"The SDS is a participant-reported outcome measure and 5 item questionnaire used for assessment of functional impairment and associated disability. First three items assess disruption of 1 work/school, 2 social life, 3 family life/home responsibilities using a 0(no impairment)-10 (most severe impairment). Score for first 3 items are summed to create total score of 0-30 where higher score indicates greater impairment and a negative change in score indicates improvement. It also has one item on days lost from school or work and one item on days when under productive. The last post baseline observation during the phase was carried forward as End Point for that phase." (NCT02418585)
Timeframe: Baseline up to Endpoint (Double-blind Induction Phase [Day 28])

InterventionUnits on a scale (Mean)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)-12.5
Intranasal Placebo Plus Oral AD-9.3

Percentage of Participants in Remission (MADRS<=12) at the Endpoint (Double-blind Induction Phase [Day 28])

"Remission was defined as participants who had a MADRS total score of less than or equal to (=<) 12. MADRS is clinician-rated scale designed to measure depression severity, and to detect changes due to antidepressant treatment. Scale consists of 10 items (apparent sadness, reported sadness, inner tension, sleep, appetite, concentration, lassitude, interest level, pessimistic thoughts, and suicidal thoughts), each of which is scored from 0 (item is not present or is normal) to 6 (severe or continuous presence of symptoms), summed for a total possible score of 0 to 60. Higher scores represent more severe condition. The last post baseline observation during the phase was carried forward as End Point for that phase." (NCT02418585)
Timeframe: At Endpoint (Double-blind Induction Phase [Day 28])

InterventionPercentage of participants (Number)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)48.2
Intranasal Placebo Plus Oral AD30.3

Percentage of Participants in Remission (SDS Total Score <=6 and Individual Item Scores Each <=2) at the End of 4-Week Double-blind Induction Phase (Day 28)

Remission defined as SDS total score <= 6 and individual item scores each <= 2. SDS is a participant reported outcome measure and is a 5-item questionnaire which has been widely used and accepted for assessment of functional impairment and associated disability. The first three items assess disruption of (1) work/school, (2) social life, and (3) family life/home responsibilities using a 0-10 rating scale. The score for the first three items were summed to create a total score of 0-30 where a higher score indicates greater impairment. It also has one item on days lost from school or work and one item on days when under productive. (NCT02418585)
Timeframe: At Day 28 (End of Double-blind Induction Phase)

InterventionPercentage of participants (Number)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)39.5
Intranasal Placebo Plus Oral AD20.9

Percentage of Participants in Response (SDS Total Score <=12 and Individual Item Scores Each <=4) at the End of 4-Week Double-blind Induction Phase (Day 28)

Response defined as SDS total score <= 12 and individual item scores each <= 4. SDS is a participant-reported outcome measure and 5 item questionnaire used for assessment of functional impairment and associated disability. First three items assess disruption of 1 work/school, 2 social life, 3 family life/home responsibilities using a 0(no impairment)-10 (most severe impairment). Score for first 3 items are summed to create total score of 0-30 where higher score indicates greater impairment and a negative change in score indicates improvement. It also has one item on days lost from school or work and one item on days when under productive. (NCT02418585)
Timeframe: At Day 28 [end of Double-blind Induction Phase]

InterventionPercentage of participants (Number)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)57.0
Intranasal Placebo Plus Oral AD39.5

Percentage of Participants Who Achieved >=50% Reduction From Baseline in MADRS Total Score at the Endpoint (Double-blind Induction Phase [Day 28])

"MADRS is clinician-rated scale designed to measure depression severity, and to detect changes due to antidepressant treatment. Scale consists of 10 items (apparent sadness, reported sadness, inner tension, sleep, appetite, concentration, lassitude, interest level, pessimistic thoughts, and suicidal thoughts), each of which is scored from 0 (item is not present or is normal) to 6 (severe or continuous presence of symptoms), summed for a total possible score of 0 to 60. Higher scores represent more severe condition. The percentage of participants with greater than or equal to (>=) 50 % reduction from baseline in MADRS total score was reported. The last post baseline observation during the phase was carried forward as End Point for that phase." (NCT02418585)
Timeframe: At Endpoint (Double-blind Induction Phase [Day 28])

InterventionPercentage of participants (Number)
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)63.4
Intranasal Placebo Plus Oral AD49.5

Percentage of Participants With Onset of Clinical Response on Day 2 and Day 8

A participant was defined as having a clinical response if there is at least 50 percent (%) improvement from baseline in the MADRS total score with onset by Day 2 and Day 8 that was maintained to Day 28. MADRS is clinician-rated scale designed to measure depression severity, and to detect changes due to antidepressant treatment. Scale consists of 10 items (apparent sadness, reported sadness, inner tension, sleep, appetite, concentration, lassitude, interest level, pessimistic thoughts, and suicidal thoughts), each of which is scored from 0 (item is not present or is normal) to 6 (severe or continuous presence of symptoms), summed for a total possible score of 0 to 60. Higher scores represent more severe condition. Participants who did not meet such criterion or discontinue during the study before Day 28 for any reason were considered as non-responders. (NCT02418585)
Timeframe: Day 2 up to Day 28 and Day 8 up to Day 28

,
InterventionPercentage of participants (Number)
Onset of Clinical response on Day 2Onset of Clinical response on Day 8
Intranasal Esketamine (Esk) Plus Oral Antidepressant (AD)7.910.5
Intranasal Placebo Plus Oral AD4.66.4

Liebowitz Social Anxiety Score (LSAS)

Clinician-administered scale for the assessment of fear and avoidance found in social phobia (SAD); it has 24 items divided into 2 subscales, 13 for performance anxiety, and 11 for social situations each rated from 0 to 3 (0=none,1=mild,2=moderate,3=definite). The sum scores for Fear and Avoidance results in an overall score (max 144 points). There are 4 clinician subscales: fear of social interaction, fear of performance, avoidance of social interaction and avoidance of performance 0 to 30= SAD is unlikely 30 to 60=SAD is probable 60 to 90=SADis very probable >90= SAD highly probable (NCT02083926)
Timeframe: Day 1 (1+28)

Interventionscore on a scale (Mean)
Ketamine Infusion on Day 0 or Day 2866.1
Saline Infusion on Day 0 or Day 2886.1

Visual Analogue Scale for Anxiety Symptoms (VAS-anxiety)

"Instrument that tries to measure anxiety, that is believed to range across a continuum of values and cannot easily be directly measured.We used a straight horizontal line of 100 mm in length. The ends were defined as the extreme limits of the parameter to be measured (anxiety); oriented from the left (no anxiety) to the right (worst anxiety ever felt). The patient marks on the line the point that they feel represents their perception of their current state.The VAS score is determined by measuring in millimeters from the left hand end of the line to the point that the patient marks.~We examined Visual Analog Scale (VAS) for anxiety symptoms at screening, 1 hour prior to infusion, 1, 2 and 3 hours after infusion, 1, 2, 3, 5, 7, 10, and 14 days following a single ketamine/saline infusion." (NCT02083926)
Timeframe: Day 1 (1+28)

Interventionunits on a scale (Mean)
Ketamine Infusion on Day 0 or Day 2812.1
Saline Infusion on Day 0 or Day 2819.6

OCD Severity

We will examine change from baseline in the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) ratings of OCD severity at 1 day following infusion. The Yale-Brown Obsessive Compulsive Scale (Y-BOCS) assesses obsessive and compulsive symptom severity. Obsessions are rated on a scale from 0-20 and compulsions are rated on a scale of 0-20, for a total scale of 0-40. Scores on the obsessions scale and scores on the compulsions scale are summed to obtain the total score. The higher the score, the more severe the OCD. (NCT01349231)
Timeframe: Baseline and 1 day after ketamine infusion

Interventionunits on a scale (Mean)
Ketamine-2.7

OCD Severity

We will examine change from baseline in the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) ratings of OCD severity at 2 days following infusion. The Yale-Brown Obsessive Compulsive Scale (Y-BOCS) assesses obsessive and compulsive symptom severity. Obsessions are rated on a scale from 0-20 and compulsions are rated on a scale of 0-20, for a total scale of 0-40. Scores on the obsessions scale and scores on the compulsions scale are summed to obtain the total score. The higher the score, the more severe the OCD. (NCT01349231)
Timeframe: Baseline and 2 days following infusion

Interventionunits on a scale (Mean)
Ketamine-3.6

OCD Severity

We will examine change from baseline in the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) ratings of OCD severity at 3 days following infusion. The Yale-Brown Obsessive Compulsive Scale (Y-BOCS) assesses obsessive and compulsive symptom severity. Obsessions are rated on a scale from 0-20 and compulsions are rated on a scale of 0-20, for a total scale of 0-40. Scores on the obsessions scale and scores on the compulsions scale are summed to obtain the total score. The higher the score, the more severe the OCD. (NCT01349231)
Timeframe: Baseline and 3 days following infusion

Interventionunits on a scale (Mean)
Ketamine-2.9

Depression Symptoms

We will examine change from baseline in Hamilton Rating Scale for Depression (HRDS) ratings of depression severity at day 1-3 following a single ketamine infusion. The HRDS assesses severity of, and change in, depressive symptoms. The HRDS is a 21 item scale with scores ranging from 0-66. The higher the score, the more severe the depression. (NCT01349231)
Timeframe: Baseline, Day 1, Day 2, and Day 3

Interventionunits on a scale (Mean)
HRDS change from Baseline to Day 1HRDS change from Baseline to Day 2HRDS change from Baseline to Day 3
Ketamine-6.57-7.29-5.14

MADRS Score - Baseline

Antidepressant effects were assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS). It is a ten-item diagnostic questionnaire which psychiatrists use to measure the severity of depressive episodes. Higher MADRS score indicates more severe depression, and each item yields a score of 0 to 6. The overall score ranges from 0 to 60. (NCT00088699)
Timeframe: Baseline

Interventionunits on a scale (Mean)
Ketamine - Healthy Volunteers1.17
Placebo - Healthy Volunteers1.48
Ketamine - MDD Patients33.83
Placebo - MDD Patients31.82

MADRS Score - Day 1 Following Intervention

Antidepressant effects were assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS). It is a ten-item diagnostic questionnaire which psychiatrists use to measure the severity of depressive episodes. Higher MADRS score indicates more severe depression, and each item yields a score of 0 to 6. The overall score ranges from 0 to 60. (NCT00088699)
Timeframe: Day 1

Interventionunits on a scale (Mean)
Ketamine - Healthy Volunteers2.45
Placebo - Healthy Volunteers0.67
Ketamine - MDD Patients23.73
Placebo - MDD Patients30.68

Reviews

17 reviews available for ketamine and Anxiety

ArticleYear
Ketamine treatment for refractory anxiety: A systematic review.
    British journal of clinical pharmacology, 2022, Volume: 88, Issue:10

    Topics: Anti-Anxiety Agents; Anxiety; Anxiety Disorders; Humans; Ketamine; Receptors, N-Methyl-D-Aspartate

2022
Neurobiological, behavioral, and cognitive effects of ketamine in adolescents: A review of human and pre-clinical research.
    Behavioural brain research, 2022, 10-28, Volume: 435

    Topics: Adolescent; Adult; Animals; Anxiety; Behavior, Animal; Cognition; Depression; Female; Humans; Ketami

2022
The role of mGlu
    Pharmacology, biochemistry, and behavior, 2022, Volume: 220

    Topics: Animals; Antidepressive Agents; Anxiety; Depression; Ketamine; Receptors, Metabotropic Glutamate

2022
Comment on 'Ketamine treatment for refractory anxiety: A systematic review'.
    British journal of clinical pharmacology, 2023, Volume: 89, Issue:6

    Topics: Anxiety; Humans; Ketamine

2023
Treatment-Resistant Late-Life Depression: A Review of Clinical Features, Neuropsychology, Neurobiology, and Treatment.
    The Psychiatric clinics of North America, 2023, Volume: 46, Issue:2

    Topics: Aged; Alzheimer Disease; Anxiety; Depressive Disorder, Treatment-Resistant; Diagnosis, Differential;

2023
Ketamine effects on anxiety and fear-related behaviors: Current literature evidence and new findings.
    Progress in neuro-psychopharmacology & biological psychiatry, 2020, 06-08, Volume: 100

    Topics: Animals; Anxiety; Avoidance Learning; Dizocilpine Maleate; Excitatory Amino Acid Antagonists; Fear;

2020
Prefrontal cortex circuits in depression and anxiety: contribution of discrete neuronal populations and target regions.
    Molecular psychiatry, 2020, Volume: 25, Issue:11

    Topics: Antidepressive Agents; Anxiety; Depression; Ketamine; Neural Pathways; Prefrontal Cortex

2020
The Canadian Network for Mood and Anxiety Treatments (CANMAT) Task Force Recommendations for the Use of Racemic Ketamine in Adults with Major Depressive Disorder: Recommandations Du Groupe De Travail Du Réseau Canadien Pour Les Traitements De L'humeur Et
    Canadian journal of psychiatry. Revue canadienne de psychiatrie, 2021, Volume: 66, Issue:2

    Topics: Adult; Antidepressive Agents; Anxiety; Canada; Depressive Disorder, Major; Humans; Ketamine

2021
Prevention and Management of Common Adverse Effects of Ketamine and Esketamine in Patients with Mood Disorders.
    CNS drugs, 2021, Volume: 35, Issue:9

    Topics: Administration, Intranasal; Administration, Intravenous; Antidepressive Agents; Anxiety; Disease Man

2021
Intranasal drug administration for procedural sedation in children admitted to pediatric Emergency Room.
    European review for medical and pharmacological sciences, 2018, Volume: 22, Issue:1

    Topics: Administration, Intranasal; Anxiety; Emergency Service, Hospital; Humans; Hypnotics and Sedatives; K

2018
Intranasal drug administration for procedural sedation in children admitted to pediatric Emergency Room.
    European review for medical and pharmacological sciences, 2018, Volume: 22, Issue:1

    Topics: Administration, Intranasal; Anxiety; Emergency Service, Hospital; Humans; Hypnotics and Sedatives; K

2018
Intranasal drug administration for procedural sedation in children admitted to pediatric Emergency Room.
    European review for medical and pharmacological sciences, 2018, Volume: 22, Issue:1

    Topics: Administration, Intranasal; Anxiety; Emergency Service, Hospital; Humans; Hypnotics and Sedatives; K

2018
Intranasal drug administration for procedural sedation in children admitted to pediatric Emergency Room.
    European review for medical and pharmacological sciences, 2018, Volume: 22, Issue:1

    Topics: Administration, Intranasal; Anxiety; Emergency Service, Hospital; Humans; Hypnotics and Sedatives; K

2018
Scientific Issues Relevant to Improving the Diagnosis, Risk Assessment, and Treatment of Major Depression.
    The American journal of psychiatry, 2019, 05-01, Volume: 176, Issue:5

    Topics: Antidepressive Agents; Anxiety; Biomedical Research; Depressive Disorder, Major; Diagnostic and Stat

2019
mGlu2/3 receptor antagonists.
    Advances in pharmacology (San Diego, Calif.), 2019, Volume: 86

    Topics: Animals; Antidepressive Agents; Anxiety; Depression; Humans; Ketamine; Receptors, Metabotropic Gluta

2019
Treatment-resistant depression: are animal models of depression fit for purpose?
    Psychopharmacology, 2015, Volume: 232, Issue:19

    Topics: Animals; Antidepressive Agents; Anxiety; Depression; Depressive Disorder, Treatment-Resistant; Disea

2015
Development of New Psychopharmacological Agents for Depression and Anxiety.
    The Psychiatric clinics of North America, 2015, Volume: 38, Issue:3

    Topics: Anti-Anxiety Agents; Antidepressive Agents; Anxiety; Botulinum Toxins; Depression; Excitatory Amino

2015
Suicide risk assessment and intervention in people with mental illness.
    BMJ (Clinical research ed.), 2015, Nov-09, Volume: 351

    Topics: Antidepressive Agents; Antipsychotic Agents; Anxiety; Cognitive Behavioral Therapy; Crisis Intervent

2015
Ketamine, propofol, and ketofol use for pediatric sedation.
    Pediatric emergency care, 2012, Volume: 28, Issue:12

    Topics: Adolescent; Amnesia; Analgesia; Analgesics, Non-Narcotic; Anesthetics, Dissociative; Antiemetics; An

2012
Management of acute pain and anxiety in children undergoing procedures in the emergency department.
    Pediatric emergency care, 2001, Volume: 17, Issue:2

    Topics: Acute Disease; Analgesia; Analgesics; Anesthesia, Local; Anxiety; Child; Child, Hospitalized; Emerge

2001

Trials

29 trials available for ketamine and Anxiety

ArticleYear
At-home, sublingual ketamine telehealth is a safe and effective treatment for moderate to severe anxiety and depression: Findings from a large, prospective, open-label effectiveness trial.
    Journal of affective disorders, 2022, 10-01, Volume: 314

    Topics: Anxiety; COVID-19; Depression; Humans; Ketamine; Pandemics; Prospective Studies; Telemedicine

2022
Analgo-Sedative Effects of Oral or Nebulized Ketamine in Preschoolers Undergoing Elective Surgery: A Comparative, Randomized, Double-Blind Study.
    Pain physician, 2020, Volume: 23, Issue:2

    Topics: Administration, Oral; Analgesics; Anesthesia Recovery Period; Anxiety; Child; Child, Preschool; Doub

2020
Using classification and regression tree modelling to investigate treatment response to a single low-dose ketamine infusion: Post hoc pooled analyses of randomized placebo-controlled and open-label trials.
    Journal of affective disorders, 2021, 02-15, Volume: 281

    Topics: Antidepressive Agents; Anxiety; Depressive Disorder, Treatment-Resistant; Humans; Infusions, Intrave

2021
The effect of esketamine in patients with treatment-resistant depression with and without comorbid anxiety symptoms or disorder.
    Depression and anxiety, 2021, Volume: 38, Issue:11

    Topics: Adult; Anxiety; Depression; Depressive Disorder, Treatment-Resistant; Double-Blind Method; Drug Ther

2021
Ketamine's dose-related effects on anxiety symptoms in patients with treatment refractory anxiety disorders.
    Journal of psychopharmacology (Oxford, England), 2017, Volume: 31, Issue:10

    Topics: Adult; Anti-Anxiety Agents; Antidepressive Agents; Anxiety; Anxiety Disorders; Depression; Depressiv

2017
Comparison of ketamine-propofol and ketamine-dexmedetomidine combinations in children for sedation during tooth extraction.
    JPMA. The Journal of the Pakistan Medical Association, 2017, Volume: 67, Issue:5

    Topics: Anesthetics, Dissociative; Anxiety; Child; Child, Preschool; Deep Sedation; Dexmedetomidine; Female;

2017
Effect of ketamine dose on self-rated dissociation in patients with treatment refractory anxiety disorders.
    Journal of psychopharmacology (Oxford, England), 2017, Volume: 31, Issue:10

    Topics: Adolescent; Anxiety; Anxiety Disorders; Dissociative Disorders; Double-Blind Method; Humans; Ketamin

2017
Pediatric premedication: a double-blind randomized trial of dexmedetomidine or ketamine alone versus a combination of dexmedetomidine and ketamine.
    BMC anesthesiology, 2017, Nov-29, Volume: 17, Issue:1

    Topics: Age Factors; Analgesics; Anxiety; Child, Preschool; Dexmedetomidine; Double-Blind Method; Drug Thera

2017
Oral Ketamine vs Placebo in Patients With Cancer-Related Neuropathic Pain: A Randomized Clinical Trial.
    JAMA oncology, 2018, 06-01, Volume: 4, Issue:6

    Topics: Aged; Analgesics; Antineoplastic Agents; Anxiety; Cancer Pain; Cognition Disorders; Depression; Doub

2018
Efficacy of intravenous ketamine treatment in anxious versus nonanxious unipolar treatment-resistant depression.
    Depression and anxiety, 2019, Volume: 36, Issue:3

    Topics: Adult; Anxiety; Anxiety Disorders; Depressive Disorder, Major; Depressive Disorder, Treatment-Resist

2019
Premedication With Midazolam or Haloperidol to Prevent Recovery Agitation in Adults Undergoing Procedural Sedation With Ketamine: A Randomized Double-Blind Clinical Trial.
    Annals of emergency medicine, 2019, Volume: 73, Issue:5

    Topics: Administration, Intravenous; Adult; Anxiety; Conscious Sedation; Double-Blind Method; Emergency Serv

2019
Premedication With Midazolam or Haloperidol to Prevent Recovery Agitation in Adults Undergoing Procedural Sedation With Ketamine: A Randomized Double-Blind Clinical Trial.
    Annals of emergency medicine, 2019, Volume: 73, Issue:5

    Topics: Administration, Intravenous; Adult; Anxiety; Conscious Sedation; Double-Blind Method; Emergency Serv

2019
Premedication With Midazolam or Haloperidol to Prevent Recovery Agitation in Adults Undergoing Procedural Sedation With Ketamine: A Randomized Double-Blind Clinical Trial.
    Annals of emergency medicine, 2019, Volume: 73, Issue:5

    Topics: Administration, Intravenous; Adult; Anxiety; Conscious Sedation; Double-Blind Method; Emergency Serv

2019
Premedication With Midazolam or Haloperidol to Prevent Recovery Agitation in Adults Undergoing Procedural Sedation With Ketamine: A Randomized Double-Blind Clinical Trial.
    Annals of emergency medicine, 2019, Volume: 73, Issue:5

    Topics: Administration, Intravenous; Adult; Anxiety; Conscious Sedation; Double-Blind Method; Emergency Serv

2019
Anxiety during ketamine infusions is associated with negative treatment responses in major depressive disorder.
    European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2019, Volume: 29, Issue:4

    Topics: Antidepressive Agents; Anxiety; Depressive Disorder, Major; Depressive Disorder, Treatment-Resistant

2019
A single infusion of ketamine improves depression scores in patients with anxious bipolar depression.
    Bipolar disorders, 2015, Volume: 17, Issue:4

    Topics: Adult; Affect; Anxiety; Anxiety Disorders; Bipolar Disorder; Cross-Over Studies; Depression; Double-

2015
Efficacy of two oral premedicants: midazolam or a low-dose combination of midazolam-ketamine for reducing stress during intravenous cannulation in children undergoing CT imaging.
    Paediatric anaesthesia, 2010, Volume: 20, Issue:4

    Topics: Administration, Oral; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Catheterization, Peri

2010
Intravenous and peritonsillar infiltration of ketamine for postoperative pain after adenotonsillectomy: a randomized placebo-controlled clinical trial.
    Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 2011, Volume: 20, Issue:5

    Topics: Adenoidectomy; Adolescent; Analysis of Variance; Anesthetics, Dissociative; Antiemetics; Anxiety; Ch

2011
Low- versus high-dose combination of midazolam-ketamine for oral premedication in children for ophthalmologic surgeries.
    Singapore medical journal, 2011, Volume: 52, Issue:7

    Topics: Anti-Anxiety Agents; Anxiety; Child; Child, Preschool; Dose-Response Relationship, Drug; Double-Blin

2011
Comparison of the effects of intranasal midazolam versus different doses of intranasal ketamine on reducing preoperative pediatric anxiety: a prospective randomized clinical trial.
    Journal of anesthesia, 2012, Volume: 26, Issue:6

    Topics: Administration, Intranasal; Anesthesia; Anxiety; Blood Pressure; Child; Child, Preschool; Conscious

2012
Ketamine psychotherapy for heroin addiction: immediate effects and two-year follow-up.
    Journal of substance abuse treatment, 2002, Volume: 23, Issue:4

    Topics: Adolescent; Adult; Anesthetics, Dissociative; Anxiety; Attitude; Depression; Double-Blind Method; Fe

2002
Ketamine plus midazolam, a most effective paediatric oral premedicant.
    Paediatric anaesthesia, 1995, Volume: 5, Issue:5

    Topics: Adjuvants, Anesthesia; Administration, Oral; Anesthesia, Inhalation; Anesthetics, Dissociative; Anxi

1995
[Analgesia-sedation for maxillo-facial surgery with midazolam-pentazocine and miazolam-ketamine. Clinical double-blind study of anxiety, analgesia, sedation and amnesia].
    Der Anaesthesist, 1995, Volume: 44, Issue:8

    Topics: Adjuvants, Anesthesia; Adult; Ambulatory Surgical Procedures; Amnesia; Analgesia; Anesthesia; Anesth

1995
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
Comparison of fentanyl/midazolam with ketamine/midazolam for pediatric orthopedic emergencies.
    Pediatrics, 1998, Volume: 102, Issue:4 Pt 1

    Topics: Adolescent; Analgesics, Opioid; Anesthetics, Dissociative; Anti-Anxiety Agents; Anxiety; Child; Chil

1998
The schizophrenia ketamine challenge study debate.
    Biological psychiatry, 1999, Oct-15, Volume: 46, Issue:8

    Topics: Anesthetics, Dissociative; Anxiety; Bioethics; Brief Psychiatric Rating Scale; Consumer Product Safe

1999
Does adjunctive midazolam reduce recovery agitation after ketamine sedation for pediatric procedures? A randomized, double-blind, placebo-controlled trial.
    Annals of emergency medicine, 2000, Volume: 35, Issue:3

    Topics: Adjuvants, Anesthesia; Adolescent; Anesthesia Recovery Period; Anesthetics, Dissociative; Anti-Anxie

2000
Does adjunctive midazolam reduce recovery agitation after ketamine sedation for pediatric procedures? A randomized, double-blind, placebo-controlled trial.
    Annals of emergency medicine, 2000, Volume: 35, Issue:3

    Topics: Adjuvants, Anesthesia; Adolescent; Anesthesia Recovery Period; Anesthetics, Dissociative; Anti-Anxie

2000
Does adjunctive midazolam reduce recovery agitation after ketamine sedation for pediatric procedures? A randomized, double-blind, placebo-controlled trial.
    Annals of emergency medicine, 2000, Volume: 35, Issue:3

    Topics: Adjuvants, Anesthesia; Adolescent; Anesthesia Recovery Period; Anesthetics, Dissociative; Anti-Anxie

2000
Does adjunctive midazolam reduce recovery agitation after ketamine sedation for pediatric procedures? A randomized, double-blind, placebo-controlled trial.
    Annals of emergency medicine, 2000, Volume: 35, Issue:3

    Topics: Adjuvants, Anesthesia; Adolescent; Anesthesia Recovery Period; Anesthetics, Dissociative; Anti-Anxie

2000
Patient anxiety scores after low-dose ketamine or fentanyl for epidural catheter placement.
    Canadian journal of anaesthesia = Journal canadien d'anesthesie, 2000, Volume: 47, Issue:9

    Topics: Adult; Analgesia, Epidural; Anesthetics, Dissociative; Anesthetics, Intravenous; Anxiety; Female; Fe

2000
Sedation for children requiring wound repair: a randomised controlled double blind comparison of oral midazolam and oral ketamine.
    Emergency medicine journal : EMJ, 2001, Volume: 18, Issue:1

    Topics: Administration, Oral; Anxiety; Child; Child, Preschool; Conscious Sedation; Dose-Response Relationsh

2001
Attenuation of ketamine effects by nimodipine pretreatment in recovering ethanol dependent men: psychopharmacologic implications of the interaction of NMDA and L-type calcium channel antagonists.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2001, Volume: 25, Issue:6

    Topics: Adult; Affect; Alcoholism; Anxiety; Blood Pressure; Calcium Channel Blockers; Calcium Channels, L-Ty

2001
A single infusion of intravenous ketamine improves pain relief in patients with critical limb ischaemia: results of a double blind randomised controlled trial.
    Pain, 2002, Volume: 97, Issue:3

    Topics: Aged; Analgesics; Analgesics, Opioid; Anxiety; Depression; Double-Blind Method; Extremities; Female;

2002
[Effects of diazepam and flunitrazepam on the undesired postoperative side-effects of ketamine anaesthesia (author's transl)].
    Der Anaesthesist, 1978, Volume: 27, Issue:6

    Topics: Adult; Anti-Anxiety Agents; Anxiety; Atropine; Diazepam; Double-Blind Method; Female; Flunitrazepam;

1978
Psychological changes in children after anaesthesia: a comparison between halothane and ketamine.
    Acta anaesthesiologica Scandinavica, 1977, Volume: 21, Issue:6

    Topics: Affective Symptoms; Anesthesia; Anxiety; Child; Child, Hospitalized; Child, Preschool; Halothane; Hu

1977

Other Studies

92 other studies available for ketamine and Anxiety

ArticleYear
Prophylactic efficacy of ketamine, but not the low-trapping NMDA receptor antagonist AZD6765, against stress-induced maladaptive behavior and 4E-BP1-related synaptic protein synthesis impairment.
    Progress in neuro-psychopharmacology & biological psychiatry, 2022, 04-20, Volume: 115

    Topics: Adaptor Proteins, Signal Transducing; Analgesics; Animals; Antidepressive Agents; Anxiety; Behavior,

2022
Ketamine acutely impairs memory consolidation and repeated exposure promotes stereotyped behavior without changing anxiety- and aggression-like parameters in adult zebrafish.
    Physiology & behavior, 2022, 04-01, Volume: 247

    Topics: Aggression; Animals; Anxiety; Behavior, Animal; Hydrocortisone; Ketamine; Memory Consolidation; Ster

2022
Ketamine sex- and dose-dependently mitigates behavioral sequelae induced by a predator-based psychosocial stress model of post-traumatic stress disorder.
    Behavioural brain research, 2022, 06-25, Volume: 428

    Topics: Animals; Anxiety; Disease Models, Animal; Female; Ketamine; Male; Rats; Rats, Sprague-Dawley; Stress

2022
Antianhedonic effects of serial intravenous subanaesthetic ketamine in anxious versus nonanxious depression.
    Journal of affective disorders, 2022, 09-15, Volume: 313

    Topics: Antidepressive Agents; Anxiety; Depression; Depressive Disorder, Major; Depressive Disorder, Treatme

2022
Clinical Effectiveness of Intravenous Racemic Ketamine Infusions in a Large Community Sample of Patients With Treatment-Resistant Depression, Suicidal Ideation, and Generalized Anxiety Symptoms: A Retrospective Chart Review.
    The Journal of clinical psychiatry, 2022, 09-12, Volume: 83, Issue:6

    Topics: Anxiety; Depression; Depressive Disorder, Major; Humans; Ketamine; Retrospective Studies; Suicidal I

2022
Real-world depression, anxiety and safety outcomes of intramuscular ketamine treatment: a retrospective descriptive cohort study.
    BMC psychiatry, 2022, 10-03, Volume: 22, Issue:1

    Topics: Adult; Anxiety; Anxiety Disorders; Cohort Studies; Depression; Depressive Disorder, Major; Humans; K

2022
The Effects of Acute and Repeated Administration of Ketamine on Memory, Behavior, and Plasma Corticosterone Levels in Female Mice.
    Neuroscience, 2023, 02-21, Volume: 512

    Topics: Animals; Anxiety; Behavior, Animal; Corticosterone; Depression; Depressive Disorder, Major; Female;

2023
The Effects of Acute and Repeated Administration of Ketamine on Memory, Behavior, and Plasma Corticosterone Levels in Female Mice.
    Neuroscience, 2023, 02-21, Volume: 512

    Topics: Animals; Anxiety; Behavior, Animal; Corticosterone; Depression; Depressive Disorder, Major; Female;

2023
The Effects of Acute and Repeated Administration of Ketamine on Memory, Behavior, and Plasma Corticosterone Levels in Female Mice.
    Neuroscience, 2023, 02-21, Volume: 512

    Topics: Animals; Anxiety; Behavior, Animal; Corticosterone; Depression; Depressive Disorder, Major; Female;

2023
The Effects of Acute and Repeated Administration of Ketamine on Memory, Behavior, and Plasma Corticosterone Levels in Female Mice.
    Neuroscience, 2023, 02-21, Volume: 512

    Topics: Animals; Anxiety; Behavior, Animal; Corticosterone; Depression; Depressive Disorder, Major; Female;

2023
One binge-type cycle of alcohol plus ketamine exposure induces emotional-like disorders associated with oxidative damage in adolescent female rats.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2023, Volume: 162

    Topics: Alcoholism; Animals; Anxiety; Ethanol; Female; Ketamine; Oxidative Stress; Prefrontal Cortex; Rats

2023
Activation of ventral hippocampal CB1 receptors inhibits ketamine-induced anxiogenic-like behavior: Alteration of BDNF/c-Fos levels in the mouse hippocampus.
    Brain research, 2023, 07-01, Volume: 1810

    Topics: Animals; Anxiety; Brain-Derived Neurotrophic Factor; Hippocampus; Ketamine; Male; Mice; Mice, Inbred

2023
The effects of ketamine on symptoms of depression and anxiety in real-world care settings: A retrospective controlled analysis.
    Journal of affective disorders, 2023, 08-15, Volume: 335

    Topics: Anxiety; Anxiety Disorders; Depression; Humans; Ketamine; Retrospective Studies

2023
A single dose of ketamine enhances early life stress-induced aggression with no effect on fear memory, anxiety-like behavior, or depression-like behavior in mice.
    Behavioral neuroscience, 2023, Volume: 137, Issue:5

    Topics: Adverse Childhood Experiences; Aggression; Animals; Anxiety; Depression; Fear; Humans; Ketamine; Mic

2023
Ketamine metabolite alleviates morphine withdrawal-induced anxiety via modulating nucleus accumbens parvalbumin neurons in male mice.
    Neurobiology of disease, 2023, 10-01, Volume: 186

    Topics: Analgesics, Opioid; Animals; Anxiety; Anxiety Disorders; Ketamine; Male; Mice; Morphine; Neurons; Nu

2023
A new approach to explore the correlation between declarative memory and anxiety in animal models of schizophrenia and microplastic pollution.
    Behavioural brain research, 2024, Feb-26, Volume: 458

    Topics: Animals; Anxiety; Ketamine; Methionine; Microplastics; Models, Animal; Plastics; Schizophrenia; Zebr

2024
Repeated intravenous infusions of ketamine: Neurocognition in patients with anxious and nonanxious treatment-resistant depression.
    Journal of affective disorders, 2019, 12-01, Volume: 259

    Topics: Adult; Antidepressive Agents; Anxiety; Depressive Disorder, Treatment-Resistant; Female; Humans; Inf

2019
NMDA receptors and L-arginine/nitric oxide/cyclic guanosine monophosphate pathway contribute to the antidepressant-like effect of Yueju pill in mice.
    Bioscience reports, 2019, 09-30, Volume: 39, Issue:9

    Topics: Animals; Antidepressive Agents; Anxiety; Arginine; Cyclic GMP; Depression; Drugs, Chinese Herbal; Hi

2019
Recovery of cognitive functioning following abstinence from ketamine.
    Addictive behaviors, 2019, Volume: 99

    Topics: Adult; Anxiety; Cognition; Cognitive Dysfunction; Depression; Excitatory Amino Acid Antagonists; Fem

2019
Association of Craving and Depressive Symptoms in Ketamine-Dependent Patients Undergoing Withdrawal Treatment.
    The American journal on addictions, 2020, Volume: 29, Issue:1

    Topics: Adolescent; Adult; Anxiety; Behavior, Addictive; Craving; Depression; Female; Humans; Ketamine; Male

2020
Sub-anesthetic and anesthetic ketamine produce different long-lasting behavioral phenotypes (24 h post-treatment) via inducing different brain-derived neurotrophic factor (BDNF) expression level in the hippocampus.
    Neurobiology of learning and memory, 2020, Volume: 167

    Topics: Animals; Anti-Anxiety Agents; Antidepressive Agents; Anxiety; Behavior, Animal; Brain-Derived Neurot

2020
A rapid positive influence of S-ketamine on the anxiety of patients in palliative care: a retrospective pilot study.
    BMC palliative care, 2020, Jan-03, Volume: 19, Issue:1

    Topics: Adult; Aged; Analysis of Variance; Anti-Anxiety Agents; Anxiety; Female; Humans; Ketamine; Male; Mid

2020
Prenatal Exposure to Ketamine Leads to Anxiety-Like Behaviors and Dysfunction in Bed Nucleus of Stria Terminalis.
    The international journal of neuropsychopharmacology, 2020, 04-21, Volume: 23, Issue:3

    Topics: Age Factors; Anesthetics, Dissociative; Animals; Anxiety; Behavior, Animal; Disease Models, Animal;

2020
Sexually Dimorphic Behavioral Profile in a Transgenic Model Enabling Targeted Recombination in Active Neurons in Response to Ketamine and (2R,6R)-Hydroxynorketamine Administration.
    International journal of molecular sciences, 2020, Mar-20, Volume: 21, Issue:6

    Topics: Animals; Anxiety; Behavior, Animal; Brain-Derived Neurotrophic Factor; Cell Nucleus; Disease Models,

2020
The effectiveness of ketamine on anxiety, irritability, and agitation: Implications for treating mixed features in adults with major depressive or bipolar disorder.
    Bipolar disorders, 2020, Volume: 22, Issue:8

    Topics: Adult; Anxiety; Bipolar Disorder; Depressive Disorder, Major; Depressive Disorder, Treatment-Resista

2020
Efficacy of low-dose ketamine infusion in anxious vs nonanxious depression: revisiting the Adjunctive Ketamine Study of Taiwanese Patients with Treatment-Resistant Depression.
    CNS spectrums, 2021, Volume: 26, Issue:4

    Topics: Adult; Antidepressive Agents; Anxiety; Depressive Disorder, Treatment-Resistant; Female; Humans; Inf

2021
Anxiolytic effects of acute and maintenance ketamine, as assessed by the Fear Questionnaire subscales and the Spielberger State Anxiety Rating Scale.
    Journal of psychopharmacology (Oxford, England), 2021, Volume: 35, Issue:2

    Topics: Anti-Anxiety Agents; Anxiety; Anxiety Disorders; Double-Blind Method; Fear; Female; Humans; Ketamine

2021
Neonatal exposure to ketamine disrupts developmental synapse unsilencing and predisposes adult mice for stressor-evoked anxiety.
    Neuropharmacology, 2020, 12-01, Volume: 180

    Topics: Age Factors; Anesthetics, Dissociative; Animals; Animals, Newborn; Anxiety; Ketamine; Long-Term Pote

2020
Facilitation of dopamine-dependent long-term potentiation in the medial prefrontal cortex of male rats follows the behavioral effects of stress.
    Journal of neuroscience research, 2021, Volume: 99, Issue:2

    Topics: Animals; Antidepressive Agents; Anxiety; Depression; Desipramine; Dopamine; Elevated Plus Maze Test;

2021
No evidence for the effectiveness of IV ketamine for treatment resistant mood disorders in retrospective study.
    Bipolar disorders, 2020, Volume: 22, Issue:8

    Topics: Adult; Anxiety; Bipolar Disorder; Depressive Disorder, Major; Depressive Disorder, Treatment-Resista

2020
The effectiveness of intravenous ketamine in adults with treatment-resistant major depressive disorder and bipolar disorder presenting with prominent anxiety: Results from the Canadian Rapid Treatment Center of Excellence.
    Journal of psychopharmacology (Oxford, England), 2021, Volume: 35, Issue:2

    Topics: Administration, Intravenous; Adult; Anxiety; Anxiety Disorders; Bipolar Disorder; Canada; Depressive

2021
Repeated subcutaneous esketamine for treatment-resistant depression: Impact of the degree of treatment resistance and anxiety comorbidity.
    Journal of psychopharmacology (Oxford, England), 2021, Volume: 35, Issue:2

    Topics: Adult; Antidepressive Agents; Anxiety; Anxiety Disorders; Comorbidity; Depression; Depressive Disord

2021
Perspectives of Ketamine Use in COVID-19 Patients.
    Journal of Korean medical science, 2021, Jan-25, Volume: 36, Issue:4

    Topics: Anesthesia; Anxiety; COVID-19; COVID-19 Drug Treatment; Critical Care; Depression; Hemodynamics; Hos

2021
Proteome profile of telencephalon associates attenuated neurogenesis with chronic stress induced mood disorder phenotypes in zebrafish model.
    Pharmacology, biochemistry, and behavior, 2021, Volume: 204

    Topics: Affect; Animals; Antidepressive Agents; Anxiety; Cell Proliferation; Depression; Disease Models, Ani

2021
Commentary on the Canadian Network for Mood and Anxiety Treatments (CANMAT) Task Force Recommendations for the Use of Racemic Ketamine in Adults with Major Depressive Disorder.
    Canadian journal of psychiatry. Revue canadienne de psychiatrie, 2021, Volume: 66, Issue:6

    Topics: Adult; Anxiety; Canada; Depressive Disorder, Major; Humans; Ketamine

2021
Low doses of ketamine and guanosine abrogate corticosterone-induced anxiety-related behavior, but not disturbances in the hippocampal NLRP3 inflammasome pathway.
    Psychopharmacology, 2021, Volume: 238, Issue:9

    Topics: Animals; Anxiety; Behavior, Animal; Corticosterone; Depression; Guanosine; Hippocampus; Inflammasome

2021
Comparative effects of sertraline, haloperidol or olanzapine treatments on ketamine-induced changes in mouse behaviours.
    Metabolic brain disease, 2017, Volume: 32, Issue:5

    Topics: Animals; Antidepressive Agents; Antipsychotic Agents; Anxiety; Behavior, Animal; Benzodiazepines; Do

2017
Behavioral Changes in Children After Emergency Department Procedural Sedation.
    Academic emergency medicine : official journal of the Society for Academic Emergency Medicine, 2018, Volume: 25, Issue:3

    Topics: Anesthetics, Dissociative; Anxiety; Chi-Square Distribution; Child; Child Behavior; Child, Preschool

2018
The effects of ketamine on sexual behavior, anxiety, and locomotion in female rats.
    Pharmacology, biochemistry, and behavior, 2018, Volume: 165

    Topics: Animals; Antidepressive Agents; Anxiety; Excitatory Amino Acid Antagonists; Female; Injections, Intr

2018
Anxiolytic effects of ascorbic acid and ketamine in mice.
    Journal of psychiatric research, 2018, Volume: 100

    Topics: Animals; Anti-Anxiety Agents; Anxiety; Ascorbic Acid; Behavior, Animal; Diazepam; Disease Models, An

2018
Ketamine Effects on EEG during Therapy of Treatment-Resistant Generalized Anxiety and Social Anxiety.
    The international journal of neuropsychopharmacology, 2018, 08-01, Volume: 21, Issue:8

    Topics: Adolescent; Adult; Aged; Anti-Anxiety Agents; Anxiety; Brain; Dose-Response Relationship, Drug; Doub

2018
Ambulatory colonoscopy under sedoanalgesia in adult patients with and without irritable bowel syndrome: A prospective, cross-sectional, and double-blind comparison.
    The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 2018, Volume: 29, Issue:3

    Topics: Aged; Analgesia; Anxiety; Colonoscopy; Cross-Sectional Studies; Dose-Response Relationship, Drug; Do

2018
Translational control of depression-like behavior via phosphorylation of eukaryotic translation initiation factor 4E.
    Nature communications, 2018, 06-25, Volume: 9, Issue:1

    Topics: Animals; Antidepressive Agents; Anxiety; Behavior, Animal; Benzofurans; Citalopram; Depression; Depr

2018
Single injection of ketamine during mid-adolescence promotes long-lasting resilience to activity-based anorexia of female mice by increasing food intake and attenuating hyperactivity as well as anxiety-like behavior.
    The International journal of eating disorders, 2018, Volume: 51, Issue:8

    Topics: Adolescent; Analgesics; Animals; Anorexia; Anxiety; Disease Models, Animal; Eating; Female; Humans;

2018
Effects of Anesthetic Ketamine on Anxiety-Like Behaviour in Rats.
    Neurochemical research, 2019, Volume: 44, Issue:4

    Topics: Anesthetics, Dissociative; Animals; Anxiety; Ketamine; Locomotion; Male; Photoperiod; Random Allocat

2019
Ketamine improved depressive-like behaviors via hippocampal glucocorticoid receptor in chronic stress induced- susceptible mice.
    Behavioural brain research, 2019, 05-17, Volume: 364

    Topics: Animals; Anxiety; Corticosterone; Depression; Depressive Disorder; Disease Models, Animal; Gene Expr

2019
Comparison of the effects of 1MeTIQ and olanzapine on performance in the elevated plus maze test and monoamine metabolism in the brain after ketamine treatment.
    Pharmacology, biochemistry, and behavior, 2019, Volume: 181

    Topics: Analysis of Variance; Animals; Antipsychotic Agents; Anxiety; Behavior, Animal; Brain; Dopamine; Dop

2019
Microglial production of quinolinic acid as a target and a biomarker of the antidepressant effect of ketamine.
    Brain, behavior, and immunity, 2019, Volume: 81

    Topics: Animals; Antidepressive Agents; Anxiety; Anxiety Disorders; Biomarkers, Pharmacological; Depression;

2019
Embryonic Ketamine Produces a Downregulation of Prefrontal Cortex NMDA Receptors and Anxiety-Like Behavior in Adult Offspring.
    Neuroscience, 2019, 09-01, Volume: 415

    Topics: Animals; Anxiety; Down-Regulation; Excitatory Amino Acid Antagonists; Female; Hindlimb Suspension; H

2019
The effects of sub-anesthetic ketamine plus ethanol on behaviors and apoptosis in the prefrontal cortex and hippocampus of adolescent rats.
    Pharmacology, biochemistry, and behavior, 2019, Volume: 184

    Topics: Anesthetics, Dissociative; Animals; Anxiety; Apoptosis; bcl-2-Associated X Protein; Behavior, Animal

2019
Chronic ketamine abuse is associated with orexin-A reduction and ACTH elevation.
    Psychopharmacology, 2020, Volume: 237, Issue:1

    Topics: Adrenocorticotropic Hormone; Adult; Anxiety; Case-Control Studies; Craving; Depressive Disorder; Fem

2020
Two cases of delayed-onset suicidal ideation, dysphoria and anxiety after ketamine infusion in patients with obsessive-compulsive disorder and a history of major depressive disorder.
    Journal of psychopharmacology (Oxford, England), 2013, Volume: 27, Issue:7

    Topics: Adult; Anxiety; Depressive Disorder, Major; Female; Humans; Ketamine; Middle Aged; Obsessive-Compuls

2013
Repeated ketamine exposure induces an enduring resilient phenotype in adolescent and adult rats.
    Biological psychiatry, 2013, Nov-15, Volume: 74, Issue:10

    Topics: Age Factors; Animals; Antidepressive Agents; Anxiety; Depression; Excitatory Amino Acid Antagonists;

2013
Cognitive impairments in poly-drug ketamine users.
    Addictive behaviors, 2013, Volume: 38, Issue:11

    Topics: Anxiety; Case-Control Studies; Cognition Disorders; Depression; Excitatory Amino Acid Antagonists; E

2013
Identification of a treatment-resistant, ketamine-sensitive genetic line in the chick anxiety-depression model.
    Pharmacology, biochemistry, and behavior, 2013, Nov-15, Volume: 113

    Topics: Animals; Anxiety; Chickens; Depression; Disease Models, Animal; Ketamine

2013
GABAA receptors containing ρ1 subunits contribute to in vivo effects of ethanol in mice.
    PloS one, 2014, Volume: 9, Issue:1

    Topics: Animals; Anxiety; Cells, Cultured; Central Nervous System Depressants; Ethanol; Female; GABA Agonist

2014
Effects of single and combined gabapentin use in elevated plus maze and forced swimming tests.
    Acta neuropsychiatrica, 2014, Volume: 26, Issue:5

    Topics: Amines; Amitriptyline; Animals; Anticonvulsants; Anxiety; Cyclohexanecarboxylic Acids; Depression; D

2014
Deletion of the Wolfram syndrome-related gene Wfs1 results in increased sensitivity to ethanol in female mice.
    Neuropharmacology, 2015, Volume: 95

    Topics: Animals; Anxiety; Central Nervous System Depressants; Dose-Response Relationship, Drug; Ethanol; Exp

2015
Low-Dose Ketamine in Chronic Critical Illness.
    Journal of intensive care medicine, 2016, Volume: 31, Issue:3

    Topics: Analgesics; Anxiety; Chronic Disease; Critical Care; Critical Illness; Dose-Response Relationship, D

2016
Ketamine as a Prophylactic Against Stress-Induced Depressive-like Behavior.
    Biological psychiatry, 2016, May-01, Volume: 79, Issue:9

    Topics: Animals; Antidepressive Agents; Anxiety; Corticosterone; Depression; Fear; Helplessness, Learned; Ke

2016
The positive effect on ketamine as a priming adjuvant in antidepressant treatment.
    Translational psychiatry, 2015, May-26, Volume: 5

    Topics: Animals; Antidepressive Agents; Anxiety; Aspartic Acid; Behavior, Animal; Brain; Depression; Depress

2015
Ketamine induces anxiolytic effects in adult zebrafish: A multivariate statistics approach.
    Behavioural brain research, 2015, Oct-01, Volume: 292

    Topics: Animals; Anti-Anxiety Agents; Anxiety; Behavior, Animal; Dose-Response Relationship, Drug; Female; K

2015
Oxytocin reduces amygdala activity, increases social interactions, and reduces anxiety-like behavior irrespective of NMDAR antagonism.
    Behavioral neuroscience, 2015, Volume: 129, Issue:4

    Topics: Amygdala; Animals; Anxiety; Brain Waves; Disease Models, Animal; Electroencephalography; Excitatory

2015
Behavioral, endocrine, and neuronal alterations in zebrafish (Danio rerio) following sub-chronic coadministration of fluoxetine and ketamine.
    Pharmacology, biochemistry, and behavior, 2015, Volume: 139 Pt B

    Topics: Animals; Antidepressive Agents, Second-Generation; Anxiety; Behavior, Animal; Brain; Depression; Dis

2015
Brain study seeks roots of suicide.
    Nature, 2015, Dec-03, Volume: 528, Issue:7580

    Topics: Anxiety; Biomarkers; Brain; Case-Control Studies; Depression; Humans; Ketamine; Risk Assessment; Ser

2015
The nitric oxide donor sodium nitroprusside attenuates recognition memory deficits and social withdrawal produced by the NMDA receptor antagonist ketamine and induces anxiolytic-like behaviour in rats.
    Psychopharmacology, 2016, Volume: 233, Issue:6

    Topics: Animals; Anti-Anxiety Agents; Anxiety; Behavior, Animal; Excitatory Amino Acid Antagonists; Ketamine

2016
Profiling the psychotic, depressive and anxiety symptoms in chronic ketamine users.
    Psychiatry research, 2016, Mar-30, Volume: 237

    Topics: Adolescent; Adult; Anxiety; China; Comorbidity; Depression; Excitatory Amino Acid Antagonists; Femal

2016
Rapamycin blocks the antidepressant effect of ketamine in task-dependent manner.
    Psychopharmacology, 2016, Volume: 233, Issue:11

    Topics: Animals; Antidepressive Agents; Anxiety; Avoidance Learning; Brain-Derived Neurotrophic Factor; Hipp

2016
Repeated ketamine treatment induces sex-specific behavioral and neurochemical effects in mice.
    Behavioural brain research, 2016, 10-01, Volume: 312

    Topics: Animals; Antidepressive Agents; Anxiety; Aspartic Acid; Depression; Female; Glutamic Acid; Hippocamp

2016
Reactive Oxygen Species-mediated Loss of Phenotype of Parvalbumin Interneurons Contributes to Long-term Cognitive Impairments After Repeated Neonatal Ketamine Exposures.
    Neurotoxicity research, 2016, Volume: 30, Issue:4

    Topics: Acetophenones; Animals; Anxiety; Brain; Cognitive Dysfunction; Cohort Studies; Disease Models, Anima

2016
Behavioral alterations of zebrafish larvae after early embryonic exposure to ketamine.
    Psychopharmacology, 2017, Volume: 234, Issue:4

    Topics: Animals; Anxiety; Avoidance Learning; Behavior, Animal; Excitatory Amino Acid Antagonists; Ketamine;

2017
Anxiolytic- and antidepressant-like properties of ketamine in behavioral and neurophysiological animal models.
    Neuroscience, 2009, Jun-30, Volume: 161, Issue:2

    Topics: Animals; Anti-Anxiety Agents; Antidepressive Agents; Anxiety; Behavior, Animal; Depression; Disease

2009
Propofol/alfentanil and propofol/ketamine procedural sedation in children with acute lymphoblastic leukaemia: safety, efficacy and their correlation with pain neuromediator expression.
    European journal of cancer care, 2010, Volume: 19, Issue:2

    Topics: Adolescent; Alfentanil; Anxiety; Child; Child, Preschool; Conscious Sedation; Cross-Over Studies; Dr

2010
Oral ketamine for the rapid treatment of depression and anxiety in patients receiving hospice care.
    Journal of palliative medicine, 2010, Volume: 13, Issue:7

    Topics: Administration, Oral; Aged; Analgesics; Antidepressive Agents; Anxiety; Depressive Disorder; Dose-Re

2010
Ketamine reduces neuronal degeneration and anxiety levels when administered during early life-induced status epilepticus in rats.
    Brain research, 2012, Sep-20, Volume: 1474

    Topics: Animals; Anxiety; Brain; Convulsants; Ketamine; Male; Nerve Degeneration; Neuroprotective Agents; Pi

2012
Opposite effects of ethanol and ketamine in the elevated plus-maze test in Wistar rats undergoing a chronic oral voluntary consumption procedure.
    Journal of psychopharmacology (Oxford, England), 2002, Volume: 16, Issue:4

    Topics: Animals; Anxiety; Behavior, Animal; Central Nervous System Depressants; Ethanol; Excitatory Amino Ac

2002
Maternal influenza infection causes marked behavioral and pharmacological changes in the offspring.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003, Jan-01, Volume: 23, Issue:1

    Topics: Acoustic Stimulation; Animals; Animals, Newborn; Antipsychotic Agents; Antiviral Agents; Anxiety; Be

2003
Ketamine-induced changes in rat behaviour: A possible animal model of schizophrenia.
    Progress in neuro-psychopharmacology & biological psychiatry, 2003, Volume: 27, Issue:4

    Topics: Anesthetics, Dissociative; Animals; Anxiety; Disease Models, Animal; Injections, Intraperitoneal; Ke

2003
Behavioral effects of ketamine and toxic interactions with psychostimulants.
    BMC neuroscience, 2006, Mar-16, Volume: 7

    Topics: Animals; Anxiety; Behavior, Animal; Central Nervous System Stimulants; Cocaine; Depression; Dose-Res

2006
Substance use and related problems: a study on the abuse of recreational and not recreational drugs in Northern Italy.
    Annali dell'Istituto superiore di sanita, 2006, Volume: 42, Issue:4

    Topics: Accidents, Traffic; Adult; Alcoholism; Amphetamines; Anxiety; Crack Cocaine; Depression; Female; Hal

2006
Premedication for outpatient adenoidectomy: comparison between ketamine and pethidine.
    The Laryngoscope, 1980, Volume: 90, Issue:3

    Topics: Adenoidectomy; Ambulatory Surgical Procedures; Anesthesia, Inhalation; Anxiety; Child, Preschool; Ev

1980
Midazolam with ketamine: who benefits?
    Annals of emergency medicine, 2000, Volume: 35, Issue:3

    Topics: Adjuvants, Anesthesia; Anesthesia Recovery Period; Anesthetics, Dissociative; Anti-Anxiety Agents; A

2000
Ketamine abusers presenting to the emergency department: a case series.
    The Journal of emergency medicine, 2000, Volume: 18, Issue:4

    Topics: Akathisia, Drug-Induced; Anesthetics, Dissociative; Anxiety; Chest Pain; Connecticut; Diagnosis, Dif

2000
Effects of ketamine on different types of anxiety/fear and related memory in rats with lesions of the median raphe nucleus.
    European journal of pharmacology, 2001, Nov-23, Volume: 431, Issue:3

    Topics: Analysis of Variance; Animals; Anxiety; Behavior, Animal; Fear; Ketamine; Male; Memory; Raphe Nuclei

2001
Effects of ketamine on patient responsiveness during the various phases of a single induced anxiety session.
    The Alabama journal of medical sciences, 1977, Volume: 14, Issue:2

    Topics: Adolescent; Adult; Anxiety; Arousal; Female; Humans; Ketamine; Male; Psychotherapy; Relaxation Thera

1977
Ketamine-facilitated induced anxiety therapy and its effect upon clients' reactions to stressful situations.
    Journal of clinical psychology, 1979, Volume: 35, Issue:2

    Topics: Adaptation, Psychological; Adolescent; Adult; Affect; Anxiety; Arousal; Depression; Female; Humans;

1979
Untoward effects of ketamine combined with diazepam for supplementing conduction anaesthesia in young and middle-aged adults.
    Acta anaesthesiologica Scandinavica, 1978, Volume: 22, Issue:6

    Topics: Adult; Age Factors; Anesthesia, Conduction; Anesthesia, Epidural; Anxiety; Confusion; Diazepam; Dose

1978
The dental treatment of problem children under ketamine analgesia.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1975, Mar-01, Volume: 49, Issue:9

    Topics: Adolescent; Analgesia; Anesthesia, Dental; Anxiety; Child; Child, Preschool; Hemophilia A; Humans; I

1975
Ketamine sedation for pediatric procedures: Part 1, A prospective series.
    Annals of emergency medicine, 1990, Volume: 19, Issue:9

    Topics: Adolescent; Anxiety; Child; Child, Preschool; Drug Evaluation; Emergency Medicine; Female; Humans; H

1990
[Control of pain and anxiety in pedodontics].
    Revista de actualidad estomatologica espanola, 1989, Volume: 49, Issue:386

    Topics: Anesthesia, Dental; Anxiety; Child; Child, Preschool; Diazepam; Humans; Hydroxyzine; Ketamine; Nitro

1989
Letter: Preoperative excitement and malignant hyperthermia.
    Lancet (London, England), 1974, Mar-16, Volume: 1, Issue:7855

    Topics: Adult; Anesthesia, General; Anxiety; Child; Humans; Injections, Intramuscular; Ketamine; Male; Malig

1974
Effect of thiopentone on emergence reactions to ketamine anaesthesia.
    Canadian Anaesthetists' Society journal, 1974, Volume: 21, Issue:3

    Topics: Anesthesia, Intravenous; Anxiety; Dreams; Female; Humans; Infusions, Parenteral; Ketamine; Thiopenta

1974
A comparison of psychologic responses to ketamine and thiopental--nitrous oxide--halothane anesthesia.
    Anesthesiology, 1972, Volume: 36, Issue:4

    Topics: Adult; Anesthetics; Anxiety; Attitude; Consciousness; Cyclohexanes; Drug Combinations; Halothane; Hu

1972
Forearm blood flow during ketamine anaesthesia.
    British journal of anaesthesia, 1972, Volume: 44, Issue:7

    Topics: Adult; Anesthesia, Inhalation; Anesthesia, Intravenous; Anxiety; Auscultation; Blood Pressure; Dilat

1972
[Avoiding of unpleasant postnarcotic dreams and anxiety with motoric restlessness following dissociation anesthesia with ketamine].
    Der Anaesthesist, 1971, Volume: 20, Issue:4

    Topics: Adolescent; Adult; Analgesics; Anxiety; Benperidol; Cyclohexanes; Dreams; Drug Antagonism; Humans; K

1971