Page last updated: 2024-10-29

ketamine and Psychoses, Drug

ketamine has been researched along with Psychoses, Drug in 81 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.

Research Excerpts

ExcerptRelevanceReference
"Ketamine mimicked the performance of schizophrenia patients on the intentional binding task, significantly increasing binding relative to placebo."9.15Ketamine administration in healthy volunteers reproduces aberrant agency experiences associated with schizophrenia. ( Absalom, AR; Adapa, R; Arana, FS; Corlett, PR; de Wit, S; Everitt, JC; Fletcher, PC; Gardner, JM; Haggard, P; Moore, JW; Morgan, HL; Pigott, JS; Turner, DC, 2011)
" 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)
"The observation that N-methyl-D-aspartate glutamate receptor (NMDAR) antagonists such as ketamine transiently induce schizophrenia-like positive, negative and cognitive symptoms has led to a paradigm shift from dopaminergic to glutamatergic dysfunction in pharmacological models of schizophrenia."8.98Glutamatergic Deficits in Schizophrenia - Biomarkers and Pharmacological Interventions within the Ketamine Model. ( Curic, S; Haaf, M; Leicht, G; Mulert, C, 2018)
"Psychotomimetics like the N-methyl-D-aspartate receptor (NMDAR) antagonist ketamine and the 5-hydroxytryptamine2A receptor (5-HT(2A)R) agonist psilocybin induce psychotic symptoms in healthy volunteers that resemble those of schizophrenia."5.16Mismatch negativity encoding of prediction errors predicts S-ketamine-induced cognitive impairments. ( Bachmann, R; Csomor, PA; Kometer, M; Schmidt, A; Seifritz, E; Stephan, KE; Vollenweider, FX, 2012)
"Ketamine mimicked the performance of schizophrenia patients on the intentional binding task, significantly increasing binding relative to placebo."5.15Ketamine administration in healthy volunteers reproduces aberrant agency experiences associated with schizophrenia. ( Absalom, AR; Adapa, R; Arana, FS; Corlett, PR; de Wit, S; Everitt, JC; Fletcher, PC; Gardner, JM; Haggard, P; Moore, JW; Morgan, HL; Pigott, JS; Turner, DC, 2011)
"Ketamine induces effects resembling both positive and negative psychotic symptoms of schizophrenia."5.13Relationship between ketamine-induced psychotic symptoms and NMDA receptor occupancy: a [(123)I]CNS-1261 SPET study. ( Arstad, E; Bressan, RA; Ell, PJ; Erlandsson, K; Krystal, JH; Pilowsky, LS; Squassante, L; Stone, JM; Teneggi, V, 2008)
" 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)
"Ketamine (1) produced behaviors similar to the positive and negative symptoms of schizophrenia; (2) elicited alterations in perception; (3) impaired performance on tests of vigilance, verbal fluency, and the Wisconsin Card Sorting Test; (4) evoked symptoms similar to dissociative states; and (5) preferentially disrupted delayed word recall, sparing immediate recall and postdistraction recall."5.07Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses. ( Bowers, MB; Bremner, JD; Charney, DS; Delaney, R; Freeman, GK; Heninger, GR; Karper, LP; Krystal, JH; Seibyl, JP, 1994)
"The observation that N-methyl-D-aspartate glutamate receptor (NMDAR) antagonists such as ketamine transiently induce schizophrenia-like positive, negative and cognitive symptoms has led to a paradigm shift from dopaminergic to glutamatergic dysfunction in pharmacological models of schizophrenia."4.98Glutamatergic Deficits in Schizophrenia - Biomarkers and Pharmacological Interventions within the Ketamine Model. ( Curic, S; Haaf, M; Leicht, G; Mulert, C, 2018)
"Over the last 20 years, glutamatergic models of schizophrenia have become increasingly accepted as etiopathological models of schizophrenia, based on the observation that phencyclidine (PCP) induces a schizophrenia-like psychosis by blocking neurotransmission at N-methyl-D-aspartate (NMDA)-type glutamate receptors."4.88Has an angel shown the way? Etiological and therapeutic implications of the PCP/NMDA model of schizophrenia. ( Heresco-Levy, U; Javitt, DC; Umbricht, D; Zukin, SR, 2012)
"The research of the glutamatergic system in schizophrenia has advanced with the use of non-competitive antagonists of glutamate NMDA receptors (phencyclidine, ketamine, and dizocilpine), which change both human and animal behaviour and induce schizophrenia-like manifestations."4.84Models of schizophrenia in humans and animals based on inhibition of NMDA receptors. ( Bubeníková-Valesová, V; Horácek, J; Höschl, C; Vrajová, M, 2008)
"Ketamine produces effects in healthy humans that resemble the positive, negative and cognitive symptoms of schizophrenia."3.81Perceptual distortions and delusional thinking following ketamine administration are related to increased pharmacological MRI signal changes in the parietal lobe. ( De Simoni, S; Dietrich, C; Kotoula, V; Krystal, JH; Mehta, MA; Stone, J, 2015)
"The aim of this study is to investigate the effects of pregabalin on the behavior of rats under the influence of ketamine, an NMDA receptor antagonist that mimics the symptoms of schizophrenia."3.78Effects of pregabalin on behavioral alterations induced by ketamine in rats. ( Baker, GB; Canever, L; Crippa, JA; Dursun, SM; Hallak, JE; Luca, RD; Nunes, EA; Oliveira, Ld; Peregrino, A; Quevedo, J; Zugno, A, 2012)
"Ketamine induced a range of perceptual distortions, but not hallucinations."3.73Psychological effects of ketamine in healthy volunteers. Phenomenological study. ( Absalom, AR; Bullmore, ET; Corlett, PR; Fletcher, PC; Honey, GD; Lee, M; McKenna, PJ; Murray, GK; Pomarol-Clotet, E, 2006)
"Ketamine was found to constitute a robust model for induction of psychomimetic symptoms and the optimal concentration range for a drug interaction study would be between 100 and 200 ng/mL."2.80Optimizing the glutamatergic challenge model for psychosis, using S+ -ketamine to induce psychomimetic symptoms in healthy volunteers. ( Dahan, A; Freijer, J; Klaassen, E; Kleinloog, D; Mooren, R; Stevens, J; Uit den Boogaard, A; van Gerven, J, 2015)
"Ketamine was associated with psychotic and dissociative symptoms."2.76Ketamine-induced disruption of verbal self-monitoring linked to superior temporal activation. ( Abel, KM; Allin, MP; Fu, CH; Matsumoto, K; McGuire, PK; Stone, JM; van Haren, N, 2011)
"Lamotrigine pretreatment prevented many of the BOLD signal changes and the symptoms."2.73Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study. ( Deakin, JF; Dursun, SM; Hallak, JE; Lees, J; McKie, S; Williams, SR, 2008)
" The magnitude of ketamine-induced changes in positive symptoms was similar, although the psychosis baseline differed, and the dose-response profiles over time were superimposable across the two populations."2.70Effects of ketamine in normal and schizophrenic volunteers. ( Lahti, AC; Parwani, A; Tamara Michaelidis, BA; Tamminga, CA; Weiler, MA, 2001)
"The frequency of psychosis emergence or confusion (54%) in Group A during the first 48 hours after surgery was significantly higher than the 30% figure in Group B."2.70Anesthesia with ketamine, propofol, and fentanyl decreases the frequency of postoperative psychosis emergence and confusion in schizophrenic patients. ( Katagai, H; Kudoh, A; Takazawa, T, 2002)
"(R)-ketamine did not produce psychotic symptoms, but a state of relaxation."2.68Differential psychopathology and patterns of cerebral glucose utilisation produced by (S)- and (R)-ketamine in healthy volunteers using positron emission tomography (PET). ( Angst, J; Hell, D; Leenders, KL; Oye, I; Vollenweider, FX, 1997)
" On several counts, the combination of ketamine and flunitrazepam was proved to reduce the adverse reactions seen with ketamine alone."2.64Reduction of psychotomimetic side effects of Ketalar (ketamine) by Rohypnol (flunitrazepam). A randomized, double-blind trial. ( Freuchen, I; Kühl, JB; Mikkelsen, BO; Ostergaard, J, 1976)
"Ketamine vs placebo was associated with enhanced neural responses in the right middle and inferior temporal gyri."1.48S-Ketamine-Induced NMDA Receptor Blockade during Natural Speech Production and Its Implications for Formal Thought Disorder in Schizophrenia: A Pharmaco-fMRI Study. ( Cabanis, M; Kircher, T; Kirner-Veselinovic, A; Nagels, A; Oppel, A; Schales, C, 2018)
"Ketamine is an anaesthetic and analgesic drug synthesized in the 1960s from phencyclidine."1.40Paliperidone for the treatment of ketamine-induced psychosis: a case report. ( Carrozzino, R; Fucile, C; Martelli, A; Mattioli, F; Muscella, A; Orengo, S; Zuccoli, ML, 2014)
"Ketamine is often used to manage neuropathic pain in patients with cancer."1.39Can gradual dose titration of ketamine for management of neuropathic pain prevent psychotomimetic effects in patients with advanced cancer? ( Matsuda, Y; Ohno, Y; Okamoto, Y; Tanimukai, H; Tsugane, M; Tsuneto, S; Uejima, E, 2013)

Research

Studies (81)

TimeframeStudies, this research(%)All Research%
pre-19908 (9.88)18.7374
1990's9 (11.11)18.2507
2000's30 (37.04)29.6817
2010's32 (39.51)24.3611
2020's2 (2.47)2.80

Authors

AuthorsStudies
Chen, ST1
Hsieh, CP1
Lee, MY1
Chen, LC1
Huang, CM1
Chen, HH1
Chan, MH1
McIntyre, RS1
Rosenblat, JD1
Nemeroff, CB1
Sanacora, G1
Murrough, JW1
Berk, M1
Brietzke, E1
Dodd, S1
Gorwood, P1
Ho, R1
Iosifescu, DV1
Lopez Jaramillo, C1
Kasper, S1
Kratiuk, K1
Lee, JG1
Lee, Y1
Lui, LMW1
Mansur, RB1
Papakostas, GI1
Subramaniapillai, M1
Thase, M1
Vieta, E1
Young, AH1
Zarate, CA1
Stahl, S1
Ma, J2
Stan Leung, L1
Leung, LS1
Nagels, A1
Cabanis, M1
Oppel, A1
Kirner-Veselinovic, A1
Schales, C1
Kircher, T1
Haaf, M1
Leicht, G1
Curic, S1
Mulert, C1
Tian, LL1
Newman, WJ1
Dong, H1
Yang, C1
Shen, Y1
Liu, L1
Liu, M1
Hao, W1
Nunes, EA1
Canever, L1
Oliveira, Ld1
Luca, RD1
Quevedo, J1
Zugno, A1
Peregrino, A1
Crippa, JA1
Dursun, SM3
Baker, GB1
Hallak, JE3
Carhart-Harris, RL1
Brugger, S1
Nutt, DJ1
Stone, JM4
Zhou, Z1
Zhang, G1
Li, X1
Liu, X1
Wang, N1
Qiu, L1
Liu, W1
Zuo, Z1
Yang, J1
Dandash, O1
Harrison, BJ1
Adapa, R3
Gaillard, R2
Giorlando, F1
Wood, SJ1
Fletcher, PC7
Fornito, A2
Xu, K1
Lipsky, RH1
Zuccoli, ML1
Muscella, A1
Fucile, C1
Carrozzino, R1
Mattioli, F1
Martelli, A1
Orengo, S1
MBSc, EN1
Joshua, N1
Morgan, C1
Rossell, SL1
Kleinloog, D1
Uit den Boogaard, A1
Dahan, A1
Mooren, R1
Klaassen, E1
Stevens, J1
Freijer, J1
van Gerven, J1
Vinckier, F1
Palminteri, S1
Rigoux, L1
Salvador, A1
Krebs, MO1
Pessiglione, M1
Stone, J1
Kotoula, V1
Dietrich, C1
De Simoni, S1
Krystal, JH6
Mehta, MA2
Francois, J1
Grimm, O1
Schwarz, AJ1
Schweiger, J1
Haller, L1
Risterucci, C1
Böhringer, A1
Zang, Z1
Tost, H1
Gilmour, G1
Meyer-Lindenberg, A1
Corlett, PR5
Honey, GD4
Steffens, M1
Becker, B1
Neumann, C1
Kasparbauer, AM1
Meyhöfer, I1
Weber, B1
Hurlemann, R1
Ettinger, U1
Khlestova, E1
Johnson, JW1
Lisman, J1
Zorumski, CF1
Izumi, Y1
Mennerick, S1
Absalom, AR4
Lee, M3
Pomarol-Clotet, E3
Murray, GK3
McKenna, PJ3
Bullmore, ET3
Menon, DK1
Daumann, J5
Heekeren, K5
Neukirch, A5
Thiel, CM2
Möller-Hartmann, W1
Gouzoulis-Mayfrank, E5
Grande Fullana, I1
To Figueras, J1
Goti Elejalde, J1
Smalla, KH1
Sahin, J1
Putzke, J1
Tischmeyer, W1
Gundelfinger, ED1
Kreutz, MR1
Wagner, D1
Sorce, S1
Schiavone, S1
Tucci, P1
Colaianna, M1
Jaquet, V1
Cuomo, V1
Dubois-Dauphin, M1
Trabace, L1
Krause, KH1
Abel, KM3
Allin, MP3
van Haren, N1
Matsumoto, K1
McGuire, PK2
Fu, CH2
Moore, JW1
Turner, DC1
Arana, FS1
Morgan, HL1
de Wit, S1
Everitt, JC1
Gardner, JM1
Pigott, JS1
Haggard, P1
Schmidt, A1
Bachmann, R1
Kometer, M1
Csomor, PA1
Stephan, KE1
Seifritz, E1
Vollenweider, FX5
D'Souza, DC2
Singh, N1
Elander, J1
Carbuto, M1
Pittman, B1
Udo de Haes, J1
Sjogren, M1
Peeters, P1
Ranganathan, M1
Schipper, J1
Chatterjee, M1
Verma, R1
Ganguly, S1
Palit, G1
Ebert, A1
Haussleiter, IS1
Juckel, G1
Brüne, M1
Roser, P1
Okamoto, Y1
Tsuneto, S1
Tanimukai, H1
Matsuda, Y1
Ohno, Y1
Tsugane, M1
Uejima, E1
Moghaddam, B1
Javitt, DC1
Zukin, SR1
Heresco-Levy, U1
Umbricht, D2
Hemsley, DR1
Geyer, MA2
Lim, DK1
Lees, J2
Deakin, JF2
Aalto, S1
Ihalainen, J1
Hirvonen, J1
Kajander, J1
Scheinin, H1
Tanila, H1
Någren, K1
Vilkman, H1
Gustafsson, LL1
Syvälahti, E1
Hietala, J1
Stoll, M2
Stock, C2
Obradovic, M2
Kovar, KA2
Perry, EB1
Gueorguieva, R1
Belger, A1
Madonick, SH1
Abi-Dargham, A1
Cooper, TB1
Macdougall, L1
Abi-Saab, W1
Gasston, D1
Costafreda, SG1
Suckling, J1
Williams, SC1
Aitken, MR1
Dickinson, A1
Shanks, DR1
Robbins, TW1
Pilowsky, LS2
Sharp, FR1
Hendren, RL1
Boeijinga, PH1
Soufflet, L1
Santoro, F1
Luthringer, R1
Covington, MA1
Riedel, WJ1
Brown, C1
He, C1
Morris, E1
Weinstein, S1
Semple, J1
Brown, J1
Tsai, GE1
Erlandsson, K1
Arstad, E1
Squassante, L1
Teneggi, V1
Bressan, RA1
Ell, PJ1
McKie, S1
Williams, SR1
Mason, OJ1
Morgan, CJ1
Stefanovic, A1
Curran, HV1
Bubeníková-Valesová, V1
Horácek, J1
Vrajová, M1
Höschl, C1
Kawohl, W1
Norra, C1
Waberski, TD1
Baer, G1
Parkas, P1
Feng, N1
Minder, EI1
Rentsch, K1
Grampp, T1
Vonderschmitt, DJ1
Karper, LP1
Seibyl, JP1
Freeman, GK1
Delaney, R1
Bremner, JD1
Heninger, GR1
Bowers, MB1
Charney, DS1
Lahti, AC2
Koffel, B1
LaPorte, D1
Tamminga, CA2
Leenders, KL2
Scharfetter, C1
Antonini, A1
Maguire, P1
Missimer, J1
Angst, J2
Oye, I1
Hell, D1
Breier, A2
Malhotra, AK2
Pinals, DA1
Weisenfeld, NI1
Pickar, D2
Goldman, D1
Picken, L1
Newcomer, JW1
Farber, NB1
Jevtovic-Todorovic, V1
Selke, G1
Melson, AK1
Hershey, T1
Craft, S1
Olney, JW1
Carpenter, WT1
Grunze, H1
Gallinat, J1
Haag, C1
Hegerl, U1
Green, SM1
Li, J1
Giannini, AJ1
Underwood, NA1
Condon, M1
Weiler, MA1
Tamara Michaelidis, BA1
Parwani, A1
Koller, R1
Schmid, L1
Kudoh, A1
Katagai, H1
Takazawa, T1
Freuchen, I1
Ostergaard, J1
Kühl, JB1
Mikkelsen, BO1
Siegel, RK1
Dipalma, JR1
Peltz, B1
Sinclair, DM1
Davidson, J1
Brewer, C1
Johnson, BD1

Clinical Trials (16)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Effect of Intravenous Low-dose Esketamine on Maternal Depression at 2 Years After Childbirth in Women With Prenatal Depression: 2-year Follow-up of a Randomized Controlled Trial[NCT05698394]Phase 4364 participants (Actual)Interventional2020-06-19Active, not recruiting
Phenomenological Explorations of the Esketamine-Induced Transient Dissociative State[NCT06133309]15 participants (Anticipated)Interventional2023-12-01Not yet recruiting
A Double-Blind, 2-Way Crossover Study to Investigate the Effects of JNJ-40411813 on Ketamine-Induced Alterations in Neuropsychiatric Performance[NCT01101659]Phase 140 participants (Actual)Interventional2010-02-28Completed
The Effects of Ketamine and Guanfacine on Working Memory in Healthy Subjects[NCT01600885]16 participants (Actual)Interventional2008-08-31Completed
Intravenous Ketamine Effects on Functional Neuroanatomy[NCT04205890]Phase 10 participants (Actual)Interventional2020-05-02Withdrawn (stopped due to Sponsor is no longer interested in funding the study)
Minocycline Augmentation of Clozapine for Treatment Resistant Schizophrenia: A Randomised Placebo-controlled Double-blind Trial[NCT02533232]Phase 160 participants (Anticipated)Interventional2022-08-30Recruiting
The Effect of a Single Dose of Lamotrigine on Brain Function in Healthy Volunteers[NCT04396938]36 participants (Actual)Interventional2017-05-10Completed
Xenon Inhalation Therapy for Major Depressive Disorder and Bipolar Disorder[NCT03748446]Early Phase 120 participants (Anticipated)Interventional2019-12-05Recruiting
Efficacy of Rapid-Acting NMDA Antagonist for Treatment of Adolescent Depression and Anxiety Disorders[NCT02579928]Phase 417 participants (Actual)Interventional2015-10-31Completed
Measurement of GABA and Neurosteroid Levels in Women With Menopausal Major Depression Before and After Treatment With Estrogen Alone, Fluoxetine Alone, or Estrogen and Fluoxetine and Normal Controls Before and After Treatment With Estrogen[NCT00626340]Phase 418 participants (Actual)Interventional1999-07-31Completed
Changes of the Short Portable Mental Status Questionnaire (SPMSQ-E) After Ketamine Administration on Ophthalmic Surgery in Geriatric Population.[NCT02049411]Phase 280 participants (Actual)Interventional2013-06-30Completed
Biomarkers of Conversion Risk and Treatment Response in Early-Stage Schizophrenia[NCT03323437]Phase 447 participants (Actual)Interventional2017-09-15Completed
Ketamine for Severe Adolescent Depression: Intermediate-term Safety and Efficacy[NCT03889756]Phase 2/Phase 33 participants (Actual)Interventional2019-07-17Terminated (stopped due to No more funding available to continue since we could not recruit throughout the pandemic.)
A Safe Ketamine-Based Therapy for Treatment Resistant Depression[NCT01179009]20 participants (Actual)Interventional2012-04-30Completed
Predictive Coding Abnormalities in Psychosis: EEG and fMRI[NCT03068806]202 participants (Actual)Observational2014-12-01Completed
Intravenous Ketamine for Pain Control During First Trimester Surgical Abortion[NCT03751423]Phase 3123 participants (Anticipated)Interventional2019-06-10Suspended (stopped due to Study on-hold due to COVID-19 pandemic restrictions. Will resume when possible.)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Percent Change in Amelioration of Ketamine-related Task Activation as Measured by Functional Magnetic Resonance Imaging in Inferior Parietal Lobule

"Scans will be analyzed for task-related prefrontal activation~Difference Score: Percent Signal Change in Regions of Interest (ketamine - saline)" (NCT01600885)
Timeframe: Within 4 hours of dose administration, after up to 1.25 hours of ketamine infusion

Interventionpercent change in saline signal (Mean)
Guanfacine-0.17
Placebo-0.094

Percent Change in Amelioration of Ketamine-related Task Activation as Measured by Functional Magnetic Resonance Imaging in Middle Frontal Gyrus

Difference Score: Percent Signal Change in Regions of Interest (ketamine - saline) (NCT01600885)
Timeframe: Within 4 hours of dose administration, after up to 1.25 hours of ketamine infusion

Interventionpercent change in saline signal (Mean)
Guanfacine-0.1
Placebo0.052

Percent Change in Amelioration of Ketamine-related Task Activation as Measured by Functional Magnetic Resonance Imaging in Superior Frontal Gyrus

Difference Score: Percent Signal Change in Regions of Interest (ketamine - saline) (NCT01600885)
Timeframe: Within 4 hours of dose administration, after up to 1.25 hours of ketamine infusion

Interventionpercent change in saline signal (Mean)
Guanfacine-0.134
Placebo-0.086

Montgomery-Asberg Depression Rating Scale Score 1 Day After Infusion

"Depressive symptoms (measured by Montgomery-Asberg Depression Rating Scale, revised (MADRS) score) on 1 day after infusion, for the cohort of subjects enrolled in the MDD arm of this trial.~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.~Usual cutoff points are:~0 to 6 - normal /symptom absent. 7 to 19 - mild depression. 20 to 34 - moderate depression. >34 - severe depression." (NCT02579928)
Timeframe: 1 day after the infusion

Interventionunits on a scale (Mean)
Ketamine15.44
Midazolam24.13

Comparison of Cortical GABA Levels in 4 Groups of Subjects Using Estrogen Alone, Fluoxetine Alone, Estrogen and Fluoxetine Combined in Pre and Post 4.0T Magnetic Resonance Spectroscopy Sessions.

"This study was conducted at Yale University almost two decades ago. Our group at the University of Pennsylvania only has very basic information about this study. This includes the number of participants, which was 18, and the fact that no adverse events occurred. Staff members at the University of Pennsylvania do not have access to any additional study data. The contact person who initially entered this study protocol information is no longer at the University of Pennsylvania and we are unable to contact for additional information.~We only know that 18 participants completed, but as far as we know data was never analyzed for these 18 participants." (NCT00626340)
Timeframe: Healthy controls will undergo scans pre and post 3 weeks of estrogen treatment. Women with depression will undergo scans pre and post 6 weeks of treatment with estrogen alone, estrogen and fluoxetine, or fluoxetine alone

Intervention ()
All Participants0

Efficacy of a Multiple-dosing Ketamine Infusion Paradigm (2 Infusions Per Week for 3 Weeks) Compared to Midazolam in Adolescents With Treatment Resistant Depression Using the Children's Depression Rating Scale (CDRS)

Establish if repeated ketamine will be efficacious medically and psychiatrically, as measured by a significant reduction in CDRS score in those treated with ketamine at the end of the dosing paradigm. The Children's Depression Rating Scale (CDRS) is a clinician-rated instrument with 17 items scored on a 1 to 5 or 1 to 7 scale. A rating of 1 indicates normal, thus the minimum score is 17. The maximum score is 113. Scores of 20-30 suggest borderline depression. Scores of 40-60 indicate moderate depression. (NCT03889756)
Timeframe: Day 18

Interventionscore on a scale (Mean)
Ketamine42
Midazolam62

Tolerability of a Multiple-dosing Ketamine Infusion Paradigm (2 Infusions Per Week for 3 Weeks) Compared to Midazolam in Adolescents With Treatment Resistant Depression

Establish if repeated ketamine will be tolerated as measured by drop-out counts. (NCT03889756)
Timeframe: Day 18

InterventionParticipants (Count of Participants)
Ketamine0
Midazolam0

Montgomery-Asberg Depression Rating Scale (MADRS) Total Score

The Montgomery-Asberg Depression Rating Scale (MADRS) is a 10-item scale that measures the severity of depression, with a higher score indicating a higher level of depression. The range of scores is 0 to 60. (NCT01179009)
Timeframe: 8 weeks

InterventionScores on a scale (Mean)
Ketamine 100-hour Infusion-9.0
Ketamine 40-minute Infusion-6.4

Reviews

8 reviews available for ketamine and Psychoses, Drug

ArticleYear
Synthesizing the Evidence for Ketamine and Esketamine in Treatment-Resistant Depression: An International Expert Opinion on the Available Evidence and Implementation.
    The American journal of psychiatry, 2021, 05-01, Volume: 178, Issue:5

    Topics: Antidepressive Agents; Delivery of Health Care; Depressive Disorder, Major; Depressive Disorder, Tre

2021
Synthesizing the Evidence for Ketamine and Esketamine in Treatment-Resistant Depression: An International Expert Opinion on the Available Evidence and Implementation.
    The American journal of psychiatry, 2021, 05-01, Volume: 178, Issue:5

    Topics: Antidepressive Agents; Delivery of Health Care; Depressive Disorder, Major; Depressive Disorder, Tre

2021
Synthesizing the Evidence for Ketamine and Esketamine in Treatment-Resistant Depression: An International Expert Opinion on the Available Evidence and Implementation.
    The American journal of psychiatry, 2021, 05-01, Volume: 178, Issue:5

    Topics: Antidepressive Agents; Delivery of Health Care; Depressive Disorder, Major; Depressive Disorder, Tre

2021
Synthesizing the Evidence for Ketamine and Esketamine in Treatment-Resistant Depression: An International Expert Opinion on the Available Evidence and Implementation.
    The American journal of psychiatry, 2021, 05-01, Volume: 178, Issue:5

    Topics: Antidepressive Agents; Delivery of Health Care; Depressive Disorder, Major; Depressive Disorder, Tre

2021
Glutamatergic Deficits in Schizophrenia - Biomarkers and Pharmacological Interventions within the Ketamine Model.
    Current pharmaceutical biotechnology, 2018, Volume: 19, Issue:4

    Topics: Animals; Biomarkers; Disease Models, Animal; Electroencephalography; Excitatory Amino Acid Antagonis

2018
Repeated ketamine administration alters N-methyl-D-aspartic acid receptor subunit gene expression: implication of genetic vulnerability for ketamine abuse and ketamine psychosis in humans.
    Experimental biology and medicine (Maywood, N.J.), 2015, Volume: 240, Issue:2

    Topics: Excitatory Amino Acid Antagonists; Gene Expression Regulation; Genetic Predisposition to Disease; Hu

2015
Prediction error, ketamine and psychosis: An updated model.
    Journal of psychopharmacology (Oxford, England), 2016, Volume: 30, Issue:11

    Topics: Animals; Association Learning; Brain; Delusions; Hallucinations; Humans; Ketamine; Psychoses, Substa

2016
Capturing the angel in "angel dust": twenty years of translational neuroscience studies of NMDA receptor antagonists in animals and humans.
    Schizophrenia bulletin, 2012, Volume: 38, Issue:5

    Topics: Allosteric Regulation; Animals; Antipsychotic Agents; Brief Psychiatric Rating Scale; Cerebral Corte

2012
Has an angel shown the way? Etiological and therapeutic implications of the PCP/NMDA model of schizophrenia.
    Schizophrenia bulletin, 2012, Volume: 38, Issue:5

    Topics: Animals; Antipsychotic Agents; Brain; Brain Mapping; Cerebral Cortex; Cognition Disorders; Contingen

2012
Psychosis: atypical limbic epilepsy versus limbic hyperexcitability with onset at puberty?
    Epilepsy & behavior : E&B, 2007, Volume: 10, Issue:4

    Topics: Adolescent; Animals; Antipsychotic Agents; Dizocilpine Maleate; Epilepsy; Excitatory Amino Acid Anta

2007
Models of schizophrenia in humans and animals based on inhibition of NMDA receptors.
    Neuroscience and biobehavioral reviews, 2008, Volume: 32, Issue:5

    Topics: Adaptation, Physiological; Animals; Disease Models, Animal; Excitatory Amino Acid Antagonists; Human

2008

Trials

35 trials available for ketamine and Psychoses, Drug

ArticleYear
Selective augmentation of striatal functional connectivity following NMDA receptor antagonism: implications for psychosis.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2015, Volume: 40, Issue:3

    Topics: Adult; Corpus Striatum; Double-Blind Method; Female; Frontal Lobe; Functional Neuroimaging; Humans;

2015
The effect of ketamine on configural facial processing.
    Journal of clinical psychopharmacology, 2015, Volume: 35, Issue:2

    Topics: Adolescent; Adult; Double-Blind Method; Excitatory Amino Acid Antagonists; Face; Female; Humans; Ket

2015
Optimizing the glutamatergic challenge model for psychosis, using S+ -ketamine to induce psychomimetic symptoms in healthy volunteers.
    Journal of psychopharmacology (Oxford, England), 2015, Volume: 29, Issue:4

    Topics: Adolescent; Adult; Cross-Over Studies; Dose-Response Relationship, Drug; Double-Blind Method; Excita

2015
Ketamine Suppresses the Ventral Striatal Response to Reward Anticipation: A Cross-Species Translational Neuroimaging Study.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2016, Volume: 41, Issue:5

    Topics: Acoustic Stimulation; Animals; Anticipation, Psychological; Brain Mapping; Conditioning, Classical;

2016
Effects of ketamine on brain function during smooth pursuit eye movements.
    Human brain mapping, 2016, Volume: 37, Issue:11

    Topics: Adult; Attention; Brain; Brain Mapping; Cerebrovascular Circulation; Double-Blind Method; Excitatory

2016
Pharmacological modulation of the neural basis underlying inhibition of return (IOR) in the human 5-HT2A agonist and NMDA antagonist model of psychosis.
    Psychopharmacology, 2008, Volume: 200, Issue:4

    Topics: Adult; Attention; Cross-Over Studies; Cues; Double-Blind Method; Female; Humans; Inhibition, Psychol

2008
Neuronal correlates of visual and auditory alertness in the DMT and ketamine model of psychosis.
    Journal of psychopharmacology (Oxford, England), 2010, Volume: 24, Issue:10

    Topics: Adult; Attention; Auditory Perception; Brain; Cross-Over Studies; Cues; Double-Blind Method; Female;

2010
Ketamine-induced disruption of verbal self-monitoring linked to superior temporal activation.
    Pharmacopsychiatry, 2011, Volume: 44, Issue:1

    Topics: Adult; Double-Blind Method; Feedback, Psychological; Humans; Ketamine; Magnetic Resonance Imaging; M

2011
Ketamine administration in healthy volunteers reproduces aberrant agency experiences associated with schizophrenia.
    Cognitive neuropsychiatry, 2011, Volume: 16, Issue:4

    Topics: Adult; Dose-Response Relationship, Drug; Excitatory Amino Acid Antagonists; Female; Healthy Voluntee

2011
Mismatch negativity encoding of prediction errors predicts S-ketamine-induced cognitive impairments.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012, Volume: 37, Issue:4

    Topics: Adult; Cognition Disorders; Double-Blind Method; Electroencephalography; Excitatory Amino Acid Antag

2012
Glycine transporter inhibitor attenuates the psychotomimetic effects of ketamine in healthy males: preliminary evidence.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012, Volume: 37, Issue:4

    Topics: Adult; Anesthetics, Dissociative; Cross-Over Studies; Glycine Plasma Membrane Transport Proteins; Hu

2012
Low dose ketamine increases prepulse inhibition in healthy men.
    Neuropharmacology, 2003, Volume: 44, Issue:6

    Topics: Acoustic Stimulation; Cognition; Cross-Over Studies; Disease Models, Animal; Double-Blind Method; El

2003
Inhibition of return in the human 5HT2A agonist and NMDA antagonist model of psychosis.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2006, Volume: 31, Issue:2

    Topics: Adult; Attention; Cross-Over Studies; Dose-Response Relationship, Drug; Double-Blind Method; Female;

2006
Comparative and interactive human psychopharmacologic effects of ketamine and amphetamine: implications for glutamatergic and dopaminergic model psychoses and cognitive function.
    Archives of general psychiatry, 2005, Volume: 62, Issue:9

    Topics: Amphetamine; Cognition; Dopamine; Double-Blind Method; Drug Interactions; Glutamine; Humans; Ketamin

2005
Effects of ketamine on prefrontal and striatal regions in an overt verbal fluency task: a functional magnetic resonance imaging study.
    Psychopharmacology, 2005, Volume: 183, Issue:1

    Topics: Corpus Striatum; Double-Blind Method; Excitatory Amino Acid Antagonists; Humans; Ketamine; Magnetic

2005
Frontal responses during learning predict vulnerability to the psychotogenic effects of ketamine: linking cognition, brain activity, and psychosis.
    Archives of general psychiatry, 2006, Volume: 63, Issue:6

    Topics: Adult; Association Learning; Brief Psychiatric Rating Scale; Cognition Disorders; Delusions; Disease

2006
Prepulse inhibition of the startle reflex and its attentional modulation in the human S-ketamine and N,N-dimethyltryptamine (DMT) models of psychosis.
    Journal of psychopharmacology (Oxford, England), 2007, Volume: 21, Issue:3

    Topics: Adult; Attention; Double-Blind Method; Excitatory Amino Acid Antagonists; Female; Hallucinogens; Hum

2007
Ketamine effects on CNS responses assessed with MEG/EEG in a passive auditory sensory-gating paradigm: an attempt for modelling some symptoms of psychosis in man.
    Journal of psychopharmacology (Oxford, England), 2007, Volume: 21, Issue:3

    Topics: Acoustic Stimulation; Adult; Auditory Perception; Double-Blind Method; Electroencephalography; Excit

2007
Does ketamine mimic aspects of schizophrenic speech?
    Journal of psychopharmacology (Oxford, England), 2007, Volume: 21, Issue:3

    Topics: Adult; Cross-Over Studies; Dose-Response Relationship, Drug; Double-Blind Method; Excitatory Amino A

2007
Relationship between ketamine-induced psychotic symptoms and NMDA receptor occupancy: a [(123)I]CNS-1261 SPET study.
    Psychopharmacology, 2008, Volume: 197, Issue:3

    Topics: Adult; Brief Psychiatric Rating Scale; Dose-Response Relationship, Drug; Guanidines; Humans; Infusio

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Glutamate and the neural basis of the subjective effects of ketamine: a pharmaco-magnetic resonance imaging study.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    Topics: Adult; Anticonvulsants; Awareness; Brain; Brief Psychiatric Rating Scale; Cross-Over Studies; Dissoc

2008
Mismatch negativity generation in the human 5HT2A agonist and NMDA antagonist model of psychosis.
    Psychopharmacology, 2008, Volume: 199, Issue:1

    Topics: Adult; Attention; Auditory Perception; Brain Mapping; Cerebral Cortex; Contingent Negative Variation

2008
Development of a gas chromatography-mass spectrometry method for determination of ketamine in plasma and its application to human samples.
    Therapeutic drug monitoring, 1995, Volume: 17, Issue:1

    Topics: Adult; Chromatography, High Pressure Liquid; Female; Gas Chromatography-Mass Spectrometry; Humans; K

1995
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses.
    Archives of general psychiatry, 1994, Volume: 51, Issue:3

    Topics: Adult; Blood Pressure; Cognition; Dissociative Disorders; Dose-Response Relationship, Drug; Double-B

1994
Subanesthetic doses of ketamine stimulate psychosis in schizophrenia.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 1995, Volume: 13, Issue:1

    Topics: Adult; Dose-Response Relationship, Drug; Double-Blind Method; Female; Glutamic Acid; Haloperidol; Hu

1995
Metabolic hyperfrontality and psychopathology in the ketamine model of psychosis using positron emission tomography (PET) and [18F]fluorodeoxyglucose (FDG).
    European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 1997, Volume: 7, Issue:1

    Topics: Adult; Brain Chemistry; Deoxyglucose; Excitatory Amino Acid Antagonists; Female; Fluorine Radioisoto

1997
Differential psychopathology and patterns of cerebral glucose utilisation produced by (S)- and (R)-ketamine in healthy volunteers using positron emission tomography (PET).
    European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 1997, Volume: 7, Issue:1

    Topics: Adult; Brain Chemistry; Cerebral Cortex; Female; Functional Laterality; Glucose; Humans; Ketamine; K

1997
The apolipoprotein E epsilon 4 allele is associated with blunting of ketamine-induced psychosis in schizophrenia. A preliminary report.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 1998, Volume: 19, Issue:5

    Topics: Adult; Affect; Apolipoprotein E4; Apolipoproteins E; Brief Psychiatric Rating Scale; Double-Blind Me

1998
Ketamine-induced NMDA receptor hypofunction as a model of memory impairment and psychosis.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 1999, Volume: 20, Issue:2

    Topics: Adult; Animals; Cognition; Depression, Chemical; Dose-Response Relationship, Drug; Double-Blind Meth

1999
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
Acute ketamine intoxication treated by haloperidol: a preliminary study.
    American journal of therapeutics, 2000, Volume: 7, Issue:6

    Topics: Adult; Anesthetics, Dissociative; Antipsychotic Agents; Double-Blind Method; Haloperidol; Humans; Ke

2000
Effects of ketamine in normal and schizophrenic volunteers.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2001, Volume: 25, Issue:4

    Topics: Adult; Behavior; Dose-Response Relationship, Drug; Excitatory Amino Acid Antagonists; Female; Humans

2001
Anesthesia with ketamine, propofol, and fentanyl decreases the frequency of postoperative psychosis emergence and confusion in schizophrenic patients.
    Journal of clinical anesthesia, 2002, Volume: 14, Issue:2

    Topics: Adult; Aged; Anesthesia, General; Anesthesia, Intravenous; Anesthetics, Dissociative; Anesthetics, I

2002
Reduction of psychotomimetic side effects of Ketalar (ketamine) by Rohypnol (flunitrazepam). A randomized, double-blind trial.
    Acta anaesthesiologica Scandinavica, 1976, Volume: 20, Issue:2

    Topics: Abortion, Induced; Adolescent; Adult; Anesthesia, Intravenous; Anti-Anxiety Agents; Blood Pressure;

1976
Induction agents for Caesarean section. A comparison of thiopentone and ketamine.
    Anaesthesia, 1973, Volume: 28, Issue:1

    Topics: Anesthesia, General; Anesthesia, Obstetrical; Apgar Score; Cesarean Section; Cognition; Dreams; Fema

1973

Other Studies

38 other studies available for ketamine and Psychoses, Drug

ArticleYear
Betaine prevents and reverses the behavioral deficits and synaptic dysfunction induced by repeated ketamine exposure in mice.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2021, Volume: 144

    Topics: Animals; Antipsychotic Agents; Behavior, Animal; Betaine; Cognition; Disease Models, Animal; Disks L

2021
Effects of GABA-B receptor positive modulator on ketamine-induced psychosis-relevant behaviors and hippocampal electrical activity in freely moving rats.
    Psychopharmacology, 2017, Volume: 234, Issue:20

    Topics: Anesthetics, Dissociative; Animals; Evoked Potentials, Auditory; GABA-B Receptor Agonists; Hippocamp

2017
Involvement of posterior cingulate cortex in ketamine-induced psychosis relevant behaviors in rats.
    Behavioural brain research, 2018, 02-15, Volume: 338

    Topics: Acoustic Stimulation; Animals; Behavior, Animal; Dose-Response Relationship, Drug; Evoked Potentials

2018
S-Ketamine-Induced NMDA Receptor Blockade during Natural Speech Production and Its Implications for Formal Thought Disorder in Schizophrenia: A Pharmaco-fMRI Study.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018, Volume: 43, Issue:6

    Topics: Adult; Brain; Brain Mapping; Cerebrovascular Circulation; Cross-Over Studies; Double-Blind Method; E

2018
Psychiatric Considerations Regarding Prehospital Administration of Ketamine for Agitation.
    The Journal of nervous and mental disease, 2019, Volume: 207, Issue:1

    Topics: Conscious Sedation; Emergency Medical Services; Humans; Hypnotics and Sedatives; Ketamine; Male; Psy

2019
Effects of ketamine use on psychotic disorders and symptoms in male, methamphetamine-dependent subjects.
    The American journal of drug and alcohol abuse, 2019, Volume: 45, Issue:3

    Topics: Adult; Amphetamine-Related Disorders; Central Nervous System Stimulants; Humans; Ketamine; Male; Met

2019
Effects of pregabalin on behavioral alterations induced by ketamine in rats.
    Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999), 2012, Volume: 34, Issue:3

    Topics: Animals; Antipsychotic Agents; Behavior, Animal; Disease Models, Animal; Dose-Response Relationship,

2012
Psychiatry's next top model: cause for a re-think on drug models of psychosis and other psychiatric disorders.
    Journal of psychopharmacology (Oxford, England), 2013, Volume: 27, Issue:9

    Topics: Amphetamine; Cannabis; Drug Users; Ethanol; Female; Humans; Ketamine; Male; Mental Disorders; Pilot

2013
Loss of phenotype of parvalbumin interneurons in rat prefrontal cortex is involved in antidepressant- and propsychotic-like behaviors following acute and repeated ketamine administration.
    Molecular neurobiology, 2015, Volume: 51, Issue:2

    Topics: Animals; Antidepressive Agents; Drug Administration Schedule; Interneurons; Ketamine; Male; Parvalbu

2015
Paliperidone for the treatment of ketamine-induced psychosis: a case report.
    International journal of psychiatry in medicine, 2014, Volume: 48, Issue:2

    Topics: Adult; Anesthetics, Dissociative; Antipsychotic Agents; Hospitalization; Humans; Isoxazoles; Ketamin

2014
Confidence and psychosis: a neuro-computational account of contingency learning disruption by NMDA blockade.
    Molecular psychiatry, 2016, Volume: 21, Issue:7

    Topics: Adult; Bayes Theorem; Conditioning, Classical; Double-Blind Method; Female; Humans; Ketamine; Learni

2016
Perceptual distortions and delusional thinking following ketamine administration are related to increased pharmacological MRI signal changes in the parietal lobe.
    Journal of psychopharmacology (Oxford, England), 2015, Volume: 29, Issue:9

    Topics: Adolescent; Adult; Anesthetics, Dissociative; Delusions; Humans; Ketamine; Magnetic Resonance Imagin

2015
The Role of GluN2C-Containing NMDA Receptors in Ketamine's Psychotogenic Action and in Schizophrenia Models.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016, 11-02, Volume: 36, Issue:44

    Topics: Animals; Brain; Evidence-Based Medicine; Hallucinogens; Humans; Ketamine; Psychoses, Substance-Induc

2016
Ketamine: NMDA Receptors and Beyond.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016, 11-02, Volume: 36, Issue:44

    Topics: Animals; Brain; Evidence-Based Medicine; Hallucinogens; Humans; Ketamine; Psychoses, Substance-Induc

2016
Individual differences in psychotic effects of ketamine are predicted by brain function measured under placebo.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008, Jun-18, Volume: 28, Issue:25

    Topics: Adult; Brain; Female; Humans; Individuality; Ketamine; Learning; Magnetic Resonance Imaging; Male; P

2008
[Ketamine-induced pychosis].
    Medicina clinica, 2008, Nov-01, Volume: 131, Issue:15

    Topics: Adult; Female; Humans; Ketamine; Psychoses, Substance-Induced

2008
Altered postsynaptic-density-levels of caldendrin in the para-chloroamphetamine-induced serotonin syndrome but not in the rat ketamine model of psychosis.
    Neurochemical research, 2009, Volume: 34, Issue:8

    Topics: Animals; Blotting, Western; Calcium-Binding Proteins; Excitatory Amino Acid Antagonists; Ketamine; M

2009
The NADPH oxidase NOX2 controls glutamate release: a novel mechanism involved in psychosis-like ketamine responses.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010, Aug-25, Volume: 30, Issue:34

    Topics: Animals; Disease Models, Animal; Glutamic Acid; Ketamine; Membrane Glycoproteins; Mice; Mice, Inbred

2010
Neurochemical and molecular characterization of ketamine-induced experimental psychosis model in mice.
    Neuropharmacology, 2012, Volume: 63, Issue:6

    Topics: Acetylcholine; Acetylcholinesterase; Amino Acids; Animals; Behavior, Animal; Biogenic Monoamines; Bi

2012
Impaired facial emotion recognition in a ketamine model of psychosis.
    Psychiatry research, 2012, Dec-30, Volume: 200, Issue:2-3

    Topics: Adult; Attention; Emotions; Excitatory Amino Acid Antagonists; Facial Expression; Humans; Ketamine;

2012
Can gradual dose titration of ketamine for management of neuropathic pain prevent psychotomimetic effects in patients with advanced cancer?
    The American journal of hospice & palliative care, 2013, Volume: 30, Issue:5

    Topics: Adolescent; Adult; Aged; Analgesics; Child; Female; Humans; Infusions, Intravenous; Ketamine; Male;

2013
Ketamine associated psychedelic effects and dependence.
    Singapore medical journal, 2003, Volume: 44, Issue:1

    Topics: Adult; Anesthetics, Dissociative; Humans; Ketamine; Male; Psychoses, Substance-Induced

2003
Gender differences and the effects of ketamine in healthy volunteers.
    Journal of psychopharmacology (Oxford, England), 2004, Volume: 18, Issue:3

    Topics: Animals; Clinical Trials as Topic; Disease Models, Animal; Female; Humans; Ketamine; Male; Psychoses

2004
Cortical glutamate-dopamine interaction and ketamine-induced psychotic symptoms in man.
    Psychopharmacology, 2005, Volume: 182, Issue:3

    Topics: Adult; Animals; Carbon Radioisotopes; Cerebral Cortex; Dopamine; Excitatory Amino Acid Antagonists;

2005
Psychological effects of ketamine in healthy volunteers. Phenomenological study.
    The British journal of psychiatry : the journal of mental science, 2006, Volume: 189

    Topics: Adult; Brief Psychiatric Rating Scale; Central Nervous System; Cognition Disorders; Delusions; Excit

2006
Psychopathological consequences of ketamine.
    The British journal of psychiatry : the journal of mental science, 2006, Volume: 189

    Topics: Adult; Brief Psychiatric Rating Scale; Delusions; Excitatory Amino Acid Antagonists; Female; Halluci

2006
Searching for rational anti N-methyl-D-aspartate treatment for depression.
    Archives of general psychiatry, 2007, Volume: 64, Issue:9

    Topics: Cognition Disorders; Depressive Disorder; Excitatory Amino Acid Antagonists; Humans; Ketamine; N-Met

2007
The psychotomimetic states inventory (PSI): measuring psychotic-type experiences from ketamine and cannabis.
    Schizophrenia research, 2008, Volume: 103, Issue:1-3

    Topics: Adolescent; Adult; Affective Symptoms; Anesthetics, Dissociative; Bipolar Disorder; Cognition Disord

2008
[Ketamine-induced psychopathological changes in normal volunteers during conditions used for experimental psychoses (author's transl)].
    Der Anaesthesist, 1981, Volume: 30, Issue:5

    Topics: Adult; Anesthesia; Female; Hallucinogens; Humans; Ketamine; Male; Psychoses, Substance-Induced; Thio

1981
Association of ketamine-induced psychosis with focal activation of the prefrontal cortex in healthy volunteers.
    The American journal of psychiatry, 1997, Volume: 154, Issue:6

    Topics: Adult; Deoxyglucose; Dose-Response Relationship, Drug; Female; Fluorine Radioisotopes; Fluorodeoxygl

1997
Psychopathological and auditory evoked potential correlates of ketamine psychosis--a single case report.
    Schizophrenia research, 2000, Jan-21, Volume: 41, Issue:2

    Topics: Anesthetics, Dissociative; Brain Mapping; Cerebral Cortex; Dominance, Cerebral; Electroencephalograp

2000
Ketamine in adults: what emergency physicians need to know about patient selection and emergence reactions.
    Academic emergency medicine : official journal of the Society for Academic Emergency Medicine, 2000, Volume: 7, Issue:3

    Topics: Adolescent; Adult; Aged; Anesthetics, Dissociative; Emergency Service, Hospital; Humans; Ketamine; M

2000
Mismatch negativity predicts psychotic experiences induced by NMDA receptor antagonist in healthy volunteers.
    Biological psychiatry, 2002, Mar-01, Volume: 51, Issue:5

    Topics: Administration, Oral; Adult; Cerebral Cortex; Contingent Negative Variation; Electroencephalography;

2002
Phencyclidine and ketamine intoxication: a study of four populations of recreational users.
    NIDA research monograph, 1978, Issue:21

    Topics: Hallucinations; Humans; Ketamine; Phencyclidine; Psychoses, Substance-Induced; Substance-Related Dis

1978
Phencyclidine: angel dust.
    American family physician, 1979, Volume: 20, Issue:1

    Topics: Adolescent; Adult; Chemical Phenomena; Chemistry; Child; Gastric Lavage; Half-Life; Humans; Illicit

1979
Psychosis and ketamine.
    British medical journal, 1972, May-06, Volume: 2, Issue:5809

    Topics: Anesthetics; Cyclohexanes; Electroconvulsive Therapy; Humans; Ketamine; Psychoses, Substance-Induced

1972
Psychosis and ketamine.
    British medical journal, 1972, Feb-12, Volume: 1, Issue:5797

    Topics: Adult; Anesthetics; Cyclohexanes; Humans; Ketamine; Preanesthetic Medication; Psychoses, Substance-I

1972
Psychosis and ketamine.
    British medical journal, 1971, Nov-13, Volume: 4, Issue:5784

    Topics: Adult; Anesthetics; Cyclohexanes; Female; Hallucinations; Humans; Ketamine; Psychoses, Substance-Ind

1971