Page last updated: 2024-11-03

riluzole and Anankastic Personality

riluzole has been researched along with Anankastic Personality in 18 studies

Riluzole: A glutamate antagonist (RECEPTORS, GLUTAMATE) used as an anticonvulsant (ANTICONVULSANTS) and to prolong the survival of patients with AMYOTROPHIC LATERAL SCLEROSIS.

Research Excerpts

ExcerptRelevanceReference
"Previous behavioral pharmacology studies involving rodents suggested riluzole had potential to be an ideal psychotropic drug for psychiatric disorders with anxiety or fear as primary symptoms."9.41Effects of riluzole on psychiatric disorders with anxiety or fear as primary symptoms: A systematic review. ( Akagi, K; Furuie, H; Kawashima, T; Kawashima, Y; Kuniishi, H; Noda, T; Yamada, M, 2023)
"The aim of the present randomized, double-blind, placebo-controlled, 8-week trial was to assess the efficacy and tolerability of riluzole augmentation of fluvoxamine in treatment of patients with moderate to severe obsessive-compulsive disorder."9.22Riluzole in augmentation of fluvoxamine for moderate to severe obsessive-compulsive disorder: Randomized, double-blind, placebo-controlled study. ( Ahmadipour, A; Akhondzadeh, S; Emamzadehfard, S; Ghaleiha, A; Kamaloo, A; Mohammadinejad, P; Paydary, K; Zeinoddini, A, 2016)
"Chronic quinpirole (QNP) sensitization is an established animal model relevant to obsessive-compulsive disorder (OCD) that has been previously shown to induce several OCD-like behavioral patterns, such as compulsive-like checking and increased locomotion."7.91No effect of riluzole and memantine on learning deficit following quinpirole sensitization - An animal model of obsessive-compulsive disorder. ( Brozka, H; Janikova, M; Radostova, D; Stuchlik, A; Svoboda, J, 2019)
"The goals of this study were to determine whether pediatric serum concentration of riluzole is similar to that observed in adults and to determine whether riluzole serum concentration is associated with adverse effects or efficacy in children and adolescents with treatment-refractory obsessive-compulsive disorder."7.85Riluzole Serum Concentration in Pediatric Patients Treated for Obsessive-Compulsive Disorder. ( Farmer, C; Grant, P; Kish, T; Song, J; Swedo, S, 2017)
"Riluzole was well tolerated; 1 patient experienced moderate nausea, but none discontinued treatment due to side effects."6.80Riluzole augmentation in treatment-refractory obsessive-compulsive disorder: a pilot randomized placebo-controlled trial. ( Billingslea, E; Bloch, MH; Coric, V; Jakubovski, E; Kelmendi, B; Pittenger, C; Sanacora, G; Simpson, R; Wasylink, S, 2015)
"Riluzole was fairly well tolerated, although it was associated with one case of pancreatitis and five instances of slight increases in transaminases."6.7912-week, placebo-controlled trial of add-on riluzole in the treatment of childhood-onset obsessive-compulsive disorder. ( Farmer, CA; Grant, PJ; Joseph, LA; Lougee, LC; Luckenbaugh, DA; Swedo, SE; Zarate, CA, 2014)
"Riluzole was well tolerated with no serious adverse effects noted."6.71Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial. ( Coric, V; Gueorguieva, R; Krystal, JH; Malison, RT; Mathalon, DH; Pittenger, C; Saksa, J; Sanacora, G; Taskiran, S; Valentine, G; Wasylink, S; Wu, YT, 2005)
"Previous behavioral pharmacology studies involving rodents suggested riluzole had potential to be an ideal psychotropic drug for psychiatric disorders with anxiety or fear as primary symptoms."5.41Effects of riluzole on psychiatric disorders with anxiety or fear as primary symptoms: A systematic review. ( Akagi, K; Furuie, H; Kawashima, T; Kawashima, Y; Kuniishi, H; Noda, T; Yamada, M, 2023)
"The aim of the present randomized, double-blind, placebo-controlled, 8-week trial was to assess the efficacy and tolerability of riluzole augmentation of fluvoxamine in treatment of patients with moderate to severe obsessive-compulsive disorder."5.22Riluzole in augmentation of fluvoxamine for moderate to severe obsessive-compulsive disorder: Randomized, double-blind, placebo-controlled study. ( Ahmadipour, A; Akhondzadeh, S; Emamzadehfard, S; Ghaleiha, A; Kamaloo, A; Mohammadinejad, P; Paydary, K; Zeinoddini, A, 2016)
" We evaluated the evidence from randomized controlled trials (RCTs) regarding the use of the glutamatergic drug riluzole in mental illnesses; and conducted preliminary meta-analyses of its effectiveness in treating obsessive-compulsive disorder (OCD) and depression."5.01Efficacy and tolerability of riluzole in psychiatric disorders: A systematic review and preliminary meta-analysis. ( Amelsvoort, TV; de Boer, JN; Hirdes, M; McAlonan, GM; Vingerhoets, C; Zinkstok, JR, 2019)
"Chronic quinpirole (QNP) sensitization is an established animal model relevant to obsessive-compulsive disorder (OCD) that has been previously shown to induce several OCD-like behavioral patterns, such as compulsive-like checking and increased locomotion."3.91No effect of riluzole and memantine on learning deficit following quinpirole sensitization - An animal model of obsessive-compulsive disorder. ( Brozka, H; Janikova, M; Radostova, D; Stuchlik, A; Svoboda, J, 2019)
"The goals of this study were to determine whether pediatric serum concentration of riluzole is similar to that observed in adults and to determine whether riluzole serum concentration is associated with adverse effects or efficacy in children and adolescents with treatment-refractory obsessive-compulsive disorder."3.85Riluzole Serum Concentration in Pediatric Patients Treated for Obsessive-Compulsive Disorder. ( Farmer, C; Grant, P; Kish, T; Song, J; Swedo, S, 2017)
"Riluzole was well tolerated; 1 patient experienced moderate nausea, but none discontinued treatment due to side effects."2.80Riluzole augmentation in treatment-refractory obsessive-compulsive disorder: a pilot randomized placebo-controlled trial. ( Billingslea, E; Bloch, MH; Coric, V; Jakubovski, E; Kelmendi, B; Pittenger, C; Sanacora, G; Simpson, R; Wasylink, S, 2015)
"Riluzole was fairly well tolerated, although it was associated with one case of pancreatitis and five instances of slight increases in transaminases."2.7912-week, placebo-controlled trial of add-on riluzole in the treatment of childhood-onset obsessive-compulsive disorder. ( Farmer, CA; Grant, PJ; Joseph, LA; Lougee, LC; Luckenbaugh, DA; Swedo, SE; Zarate, CA, 2014)
"Riluzole was well tolerated with no serious adverse effects noted."2.71Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial. ( Coric, V; Gueorguieva, R; Krystal, JH; Malison, RT; Mathalon, DH; Pittenger, C; Saksa, J; Sanacora, G; Taskiran, S; Valentine, G; Wasylink, S; Wu, YT, 2005)

Research

Studies (18)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's6 (33.33)29.6817
2010's10 (55.56)24.3611
2020's2 (11.11)2.80

Authors

AuthorsStudies
Kawashima, Y1
Yamada, M2
Furuie, H1
Kuniishi, H1
Akagi, K1
Kawashima, T1
Noda, T1
Janikova, M2
Mainerova, K1
Vojtechova, I1
Petrasek, T1
Svoboda, J2
Stuchlik, A2
Grant, P3
Farmer, C1
Song, J1
Kish, T1
Swedo, S1
Brozka, H1
Radostova, D1
de Boer, JN1
Vingerhoets, C1
Hirdes, M1
McAlonan, GM1
Amelsvoort, TV1
Zinkstok, JR1
Rapp, A1
Dodds, A1
Walkup, JT1
Rynn, M1
Grant, PJ1
Joseph, LA1
Farmer, CA1
Luckenbaugh, DA1
Lougee, LC1
Zarate, CA1
Swedo, SE3
Pittenger, C4
Bloch, MH2
Wasylink, S4
Billingslea, E1
Simpson, R1
Jakubovski, E1
Kelmendi, B3
Sanacora, G2
Coric, V5
Emamzadehfard, S1
Kamaloo, A1
Paydary, K1
Ahmadipour, A1
Zeinoddini, A2
Ghaleiha, A1
Mohammadinejad, P1
Akhondzadeh, S1
Song, JY1
Mahgoub, N1
Asemota, B1
Alexopoulos, GS1
Vloet, TD1
Simons, M1
Herpertz-Dahlmann, B1
Milanovic, S1
Patel, P1
Malison, R1
Krystal, JH3
Taskiran, S1
Mathalon, DH1
Valentine, G1
Saksa, J1
Wu, YT1
Gueorguieva, R1
Malison, RT2
Sasso, DA1
Kalanithi, PS1
Trueblood, KV1
Wayslink, S1
Lougee, L1
Hirschtritt, M1
Egashira, N1
Okuno, R1
Harada, S1
Matsushita, M1
Mishima, K1
Iwasaki, K1
Nishimura, R1
Oishi, R1
Fujiwara, M1

Clinical Trials (7)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Dextromethorphan as an Augmentation Agent in Treatment-resistant Schizophrenia: A Randomized, Group Sequential Adaptive Design, Controlled Clinical Trial[NCT05944510]Phase 472 participants (Anticipated)Interventional2023-08-31Recruiting
An Investigation of the Efficacy in Childhood Obsessive-Compulsive Disorder of Riluzole: An Antiglutamatergic Agent[NCT00251303]Phase 278 participants (Actual)Interventional2005-08-31Completed
A Double-blind Study of Riluzole Augmentation in Serotonin Reuptake Inhibitor-refractory Obsessive-compulsive Disorder and Depression[NCT00523718]Phase 240 participants (Actual)Interventional2006-09-30Completed
Ketamine Treatment for Pediatric-Refractory Obsessive-Compulsive Disorder (OCD)[NCT02422290]Phase 1/Phase 25 participants (Actual)Interventional2015-03-31Completed
Augment in Treatment-resistent Obsessive-compulsive Disorder: an Open-label Trial[NCT00590642]30 participants (Anticipated)Observational2006-04-30Completed
A Double-Blind, Placebo-controlled Pilot Study of NAC Addition to Dialectical Behavioral Therapy for the Treatment of Self-Injurious Behavior Associated With Borderline Personality Disorder[NCT00539188]Phase 26 participants (Actual)Interventional2007-09-30Terminated (stopped due to Study terminated due to poor subject compliance.)
A Double-Blind Study of N-Acetylcysteine Augmentation in Serotonin Reuptake Inhibitor-Refractory Obsessive-Compulsive Disorder and Depression[NCT00539513]Phase 210 participants (Actual)Interventional2006-06-30Terminated (stopped due to Researchers terminated study due to limited enrollment.)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Children's Yale-Brown Obsessive-Compulsive Scale Scores (CY-BOCS)

CY-BOCS is a 0-40 point scale of obsessive-compulsive symptom severity, higher number indicates more severe obsessive-compulsive symptoms. Comparison of 12 weeks scores for placebo and riluzole groups. (NCT00251303)
Timeframe: 12 weeks

Interventionunits on a scale (Mean)
Riluzole21.72
Placebo23.30

Much/Very Much Improved on Clinical Global Impressions - Improvement Score (CGI-I)

(NCT00251303)
Timeframe: 12 weeks

Interventionparticipants (Number)
Riluzole3
Placebo4

Average Hamilton Anxiety Inventory (HAM-A)

The Hamilton Anxiety Rating Scale (HARS or HAM-A) is a psychological questionnaire used by clinicians to rate the severity of a patient's anxiety. Total score ranges from 0 to 56. A score of 17 or less indicates mild anxiety severity. A score from 18 to 24 indicates mild to moderate anxiety severity. A score of 25 to 30 indicates a moderate to severe anxiety severity. A score of 31 or greater represents very severe anxiety severity. (NCT00523718)
Timeframe: 14 weeks

Interventionunits on a scale (Mean)
Riluzole14.176
Placebo14.263

Average Hamilton Depression Inventory (HAM-D)

"The HDRS (also known as the HAM-D) is the most widely used clinician-administered depression assessment scale. The HAM-D 17-item scale ranges from 0 (normal) to >23 (very severe depression), with a maximum score of 52. The 24-item scale has a maximum score of 75. Severity of depression (e.g. normal or very severe) is based upon the score in the first 17-items." (NCT00523718)
Timeframe: 14 weeks

Interventionunits on a scale (Mean)
Riluzole11.941
Placebo12.53

Clinical Global Impression (CGI) - Severity of Illness Item

The Clinical Global Impression - Severity scale (CGI-S) is a 7-point scale that requires the clinician to rate the severity of the patient's illness at the time of assessment, relative to the clinician's past experience with patients who have the same diagnosis. Considering total clinical experience, a patient is assessed on severity of mental illness at the time of rating 1, normal, not at all ill; 2, borderline mentally ill; 3, mildly ill; 4, moderately ill; 5, markedly ill; 6, severely ill; or 7, extremely ill. (NCT00523718)
Timeframe: 14 weeks

Interventionunits on a scale (Mean)
Riluzole3.94
Placebo3.95

Partial Responders by Yale-Brown Obsessive-Compulsive Scale (Y-BOCS)

"The Yale-Brown Obsessive Compulsive Scale (Y-BOCS) is a test to rate the severity of obsessive-compulsive disorder (OCD) symptoms. The scale is a clinician-rated, 10-item scale, each item rated from 0 (no symptoms) to 4 (extreme symptoms), yielding a total possible score range from 0 to 40. The results can be interpreted based on the total score:~0-7 is sub-clinical; 8-15 is mild; 16-23 is moderate; 24-31 is severe; 32-40 is extreme.~Improvement was defined apriori as a 25% improvement from baseline" (NCT00523718)
Timeframe: 14 weeks

Interventionparticipants (Number)
Riluzole5
Placebo2

Children's Yale-Brown Obsessive Compulsive Scale (CY-BOCS)

The CY-BOCS is a semi-structured measure of OCD severity with excellent inter-rater reliability, internal consistency, and test-retest reliability. It is validated in those starting at age 7 and used in studies up to age 20. The CYBOCS differs from the adult YBOCS only in its use of simpler language. The CY-BOCS consists of 10 items which are summed up to derive the total CY-BOCS score. The total score ranges from 0-40 with higher scores indicating greater severity of OCD symptoms. (NCT02422290)
Timeframe: Screening, Baseline, Day 7, Day 17, 3-Month; Baseline and Day 14 pre-specified to be reported

Interventionscore on a scale (Mean)
CY-BOCS BaselineCY-BOCS Day 14
Ketamine Treatment Group29.0026.20

Clinical Global Impressions - Severity Scale (CGI-S)

The CGI-S is a clinician rated 7-point rating scale for the severity of a participant's illness relative to the clinician's experience of working with this particular population. The score ranges from 1-7 with higher scores indicating greater illness severity. (NCT02422290)
Timeframe: Screening, Baseline, Day 7, Day 17, 3-Month; Baseline and Day 14 pre-specified to be reported

Interventionscore on a scale (Mean)
CGI-S BaselineCGI-S Day 14
Ketamine Treatment Group5.805.00

OCD Visual Analogue Scale (OCD-VAS)

"The OCD-VAS is a one-item unipolar scale to assess OCD symptoms over a rapid time frame (No obsessions to Constant obsessions). The scale ranges from 0-10 with higher scores indicating higher presence of obsessions." (NCT02422290)
Timeframe: Screening, Baseline, Day 1-14, 3-Month; Baseline and Day 14 pre-specified to be reported

Interventionscore on a scale (Mean)
OCD-VAS BaselineOCD-VAS Day 14
Ketamine Treatment Group5.005.00

Yale-Brown Obsessive Compulsive Challenge Scale (Y-BOCCS)

"The Y-BOCCS is self-report scale which assesses OCD symptoms on a 5-point likert scale (None to Extreme). It consists of 10 items which are summed up to derive the total Y-BOCCS score. The total score ranges from 0-40 with higher scores indicating higher prevalence of OCD symptoms." (NCT02422290)
Timeframe: Screening, Baseline, Day 1-14, 3-Month; Baseline and Day 14 pre-specified to be reported

Interventionscore on a scale (Mean)
Y-BOCCS BaselineY-BOCCS Day 14
Ketamine Treatment Group18.2516.50

Hamilton Depression Rating Scale (HAM-D) at 6 Weeks

"The Hamilton Rating Scale for Depression is a multiple item questionnaire used to provide an indication of depression, and as a guide to evaluate recovery. Administered by a clinician, The questionnaire is designed for adults and is used to rate the severity of the patients depression by asking their mood, feelings of guilt, insomnia, agitation, weight change, suicidal ideation, and somatic symptoms. The scale also allows the clinician to assess the patient's level of retardation, and insight into their depression. Highest possible score is 52.~HAM-D Scoring 0-7 = Normal 8-13 = Mild Depression 14-18 = Moderate Depression 19-22 = Severed Depression~≥23 = Very Severe Depression~In this study, Baseline ratings were compared to those of week 6 to assess each participants change in depression throughout the study. A negative value indicates an increase in depression (i.e. the individual felt more depressed) and a positive value indicates a decrease in depression." (NCT00539188)
Timeframe: 6 weeks

Interventionunits on a scale (Number)
N-Acetylcysteine28
Placebo18

Hamilton Depression Rating Scale (HAM-D) at Baseline

"The Hamilton Rating Scale for Depression is a multiple item questionnaire used to provide an indication of depression, and as a guide to evaluate recovery. Administered by a clinician, The questionnaire is designed for adults and is used to rate the severity of the patients depression by asking their mood, feelings of guilt, insomnia, agitation, weight change, suicidal ideation, and somatic symptoms. The scale also allows the clinician to assess the patient's level of retardation, and insight into their depression. Highest possible score is 52.~HAM-D Scoring 0-7 = Normal 8-13 = Mild Depression 14-18 = Moderate Depression 19-22 = Severed Depression~≥23 = Very Severe Depression~In this study, Baseline ratings were compared to those of week 6 to assess each participants change in depression throughout the study. A negative value indicates an increase in depression (i.e. the individual felt more depressed) and a positive value indicates a decrease in depression." (NCT00539188)
Timeframe: Baseline

Interventionunits on a scale (Number)
N-Acetylcysteine25
Placebo27

Self-Harm Inventory (SHI) Score at 6 Weeks

"The Self-Harm Inventory is assessed by asking an individual to answer (yes or no) if they have ever intentionally, or on purpose tried to harm themselves. The inventory contains 22 questions and a 23rd marked other that allows the individual to indicate a self-harm behavior not previously mentioned.~The scoring of this instrument is determined by counting the number of endorsed self-harm behaviors out of the possible twenty-three asked. The maximum score any individual may achieve for the SHI is a 23. Any individual scoring 5 or greater is classified as suffering from BPD.~In this study, scoring on the SHI was primarily used to assess improvement of self-harming symptoms and throughout the study by comparing participant ratings from baseline and week 6. Positive numbers indicate a decrease (i.e. participant indicated less self-harming behavior) and negative numbers indicate an increase in self-harming behaviors reported." (NCT00539188)
Timeframe: 6 weeks

Interventionunits on a scale (Number)
N-Acetylcysteine5
Placebo1

Self-Harm Inventory (SHI) Score at Baseline

"The Self-Harm Inventory is assessed by asking an individual to answer (yes or no) if they have ever intentionally, or on purpose tried to harm themselves. The inventory contains 22 questions and a 23rd marked other that allows the individual to indicate a self-harm behavior not previously mentioned.~The scoring of this instrument is determined by counting the number of endorsed self-harm behaviors out of the possible twenty-three asked. The maximum score any individual may achieve for the SHI is a 23. Any individual scoring 5 or greater is classified as suffering from BPD.~In this study, scoring on the SHI was primarily used to assess improvement of self-harming symptoms and throughout the study by comparing participant ratings from baseline and week 6. Positive numbers indicate a decrease (i.e. participant indicated less self-harming behavior) and negative numbers indicate an increase in self-harming behaviors reported." (NCT00539188)
Timeframe: Baseline

Interventionunits on a scale (Number)
N-Acetylcysteine8
Placebo4

The Hamilton Depression Inventory (HAM-D)at 12 Weeks

"The Hamilton Rating Scale for Depression is a multiple item (traditionally 17) assessment used to provide an indication of depression and as a guide to evaluate recovery. The clinician-rated assessment is designed for adults and is used to rate the severity of patient depression by asking about mood, feelings of guilt, insomnia, agitation, weight change, suicidal ideation, and somatic symptoms. The scale also allows the clinician to assess the patient's level of retardation, and insight into their depression.~In this study, the HAM-D17 (17 items scored) was used to obtain depression severity ratings with a maximum possible score of 52. Baseline ratings are compared to those of week 12 to produce a percentage of change, where positive values indicate a decrease in depressive severity/symptoms. Maximum score is a 52.~Ranges~0-7 = Normal 8-13 = Mild Depression 14-18 = Moderate Depression 19-22 = Severe Depression~≥23 = Very Severe Depression" (NCT00539513)
Timeframe: 12 weeks

Interventionunits on a scale (Mean)
N-Acetylcysteine12.1
Placebo7.0

The Hamilton Depression Inventory (HAM-D)at Baseline

"The Hamilton Rating Scale for Depression is a multiple item (traditionally 17) assessment used to provide an indication of depression and as a guide to evaluate recovery. The clinician-rated assessment is designed for adults and is used to rate the severity of patient depression by asking about mood, feelings of guilt, insomnia, agitation, weight change, suicidal ideation, and somatic symptoms. The scale also allows the clinician to assess the patient's level of retardation, and insight into their depression.~In this study, the HAM-D17 (17 items scored) was used to obtain depression severity ratings with a maximum possible score of 52. Baseline ratings are compared to those of week 12 to produce a percentage of change, where positive values indicate a decrease in depressive severity/symptoms. Maximum score is a 52.~Ranges~0-7 = Normal 8-13 = Mild Depression 14-18 = Moderate Depression 19-22 = Severe Depression~≥23 = Very Severe Depression" (NCT00539513)
Timeframe: Baseline

Interventionunits on a scale (Mean)
N-Acetylcysteine17.3
Placebo8.7

Yale-Brown Obsessive-Compulsive Scale (Y-BOCS)at 12 Weeks

"The Y-BOCS is a 10 item clinician-rated scale used to both determine the severity of OCD and to monitor symptom improvement throughout the course of the study. The Y-BOCS, specifically measures the severity of symptoms of obsessive-compulsive disorder without being biased towards the type of obsessions or compulsions present. The scale includes questions about the amount of time spent on, how much impairment or distress experienced from, and how much resistance and control over these obsessive thoughts and compulsions.~Each item is rated from 0 (no symptoms) to 4 (extreme symptoms) and yields a total possible score range from 0 to 40, with the following ranges indicating degree of severity:~0-7 = sub-clinical 8-15 = mild 16-23 = moderate 24-31 = severe 32-40 = extreme~In this study, baseline ratings are compared to those of week 12 to produce a percent of change with positive percentages indicating a decrease in symptom severity." (NCT00539513)
Timeframe: 12 Weeks

Interventionunits on a scale (Mean)
N-Acetylcysteine30.6
Placebo28.7

Yale-Brown Obsessive-Compulsive Scale (Y-BOCS)at Baseline

"The Y-BOCS is a 10 item clinician-rated scale used to both determine the severity of OCD and to monitor symptom improvement throughout the course of the study. The Y-BOCS, specifically measures the severity of symptoms of obsessive-compulsive disorder without being biased towards the type of obsessions or compulsions present. The scale includes questions about the amount of time spent on, how much impairment or distress experienced from, and how much resistance and control over these obsessive thoughts and compulsions.~Each item is rated from 0 (no symptoms) to 4 (extreme symptoms) and yields a total possible score range from 0 to 40, with the following ranges indicating degree of severity:~0-7 = sub-clinical 8-15 = mild 16-23 = moderate 24-31 = severe 32-40 = extreme~In this study, baseline ratings are compared to those of week 12 to produce a percent of change with positive percentages indicating a decrease in symptom severity." (NCT00539513)
Timeframe: Baseline

Interventionunits on a scale (Mean)
N-Acetylcysteine30.3
Placebo28.6

Reviews

5 reviews available for riluzole and Anankastic Personality

ArticleYear
Effects of riluzole on psychiatric disorders with anxiety or fear as primary symptoms: A systematic review.
    Neuropsychopharmacology reports, 2023, Volume: 43, Issue:3

    Topics: Anxiety; Anxiety Disorders; Fear; Humans; Obsessive-Compulsive Disorder; Riluzole

2023
Efficacy and tolerability of riluzole in psychiatric disorders: A systematic review and preliminary meta-analysis.
    Psychiatry research, 2019, Volume: 278

    Topics: Adult; Autistic Disorder; Depressive Disorder; Female; Humans; Male; Mental Disorders; Neuroprotecti

2019
Treatment of pediatric anxiety disorders.
    Annals of the New York Academy of Sciences, 2013, Volume: 1304

    Topics: Adolescent; Anticonvulsants; Anxiety Disorders; Anxiety, Separation; Child; Cognitive Behavioral The

2013
Review of the use of the glutamate antagonist riluzole in psychiatric disorders and a description of recent use in childhood obsessive-compulsive disorder.
    Journal of child and adolescent psychopharmacology, 2010, Volume: 20, Issue:4

    Topics: Adult; Age Factors; Animals; Child; Clinical Trials as Topic; Excitatory Amino Acid Antagonists; Hum

2010
[Psychotherapeutic and pharmacological treatment of pediatric obsessive-compulsive disorder].
    Zeitschrift fur Kinder- und Jugendpsychiatrie und Psychotherapie, 2012, Volume: 40, Issue:1

    Topics: Adolescent; Antipsychotic Agents; Child; Clomipramine; Cognitive Behavioral Therapy; Combined Modali

2012

Trials

5 trials available for riluzole and Anankastic Personality

ArticleYear
12-week, placebo-controlled trial of add-on riluzole in the treatment of childhood-onset obsessive-compulsive disorder.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2014, Volume: 39, Issue:6

    Topics: Adolescent; Age of Onset; Child Development Disorders, Pervasive; Comorbidity; Double-Blind Method;

2014
Riluzole augmentation in treatment-refractory obsessive-compulsive disorder: a pilot randomized placebo-controlled trial.
    The Journal of clinical psychiatry, 2015, Volume: 76, Issue:8

    Topics: Adult; Drug Synergism; Drug Therapy, Combination; Excitatory Amino Acid Antagonists; Female; Humans;

2015
Riluzole in augmentation of fluvoxamine for moderate to severe obsessive-compulsive disorder: Randomized, double-blind, placebo-controlled study.
    Psychiatry and clinical neurosciences, 2016, Volume: 70, Issue:8

    Topics: Adult; Double-Blind Method; Drug Synergism; Drug Therapy, Combination; Excitatory Amino Acid Antagon

2016
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
Riluzole augmentation in treatment-resistant obsessive-compulsive disorder: an open-label trial.
    Biological psychiatry, 2005, Sep-01, Volume: 58, Issue:5

    Topics: Adult; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Middle Aged; Obsess

2005
An open-label trial of riluzole, a glutamate antagonist, in children with treatment-resistant obsessive-compulsive disorder.
    Journal of child and adolescent psychopharmacology, 2007, Volume: 17, Issue:6

    Topics: Adolescent; Child; Drug Resistance; Excitatory Amino Acid Antagonists; Female; Humans; Male; Obsessi

2007

Other Studies

8 other studies available for riluzole and Anankastic Personality

ArticleYear
Memantine and Riluzole Exacerbate, Rather Than Ameliorate Behavioral Deficits Induced by 8-OH-DPAT Sensitization in a Spatial Task.
    Biomolecules, 2021, 07-09, Volume: 11, Issue:7

    Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Animals; Behavior, Animal; Disease Models, Animal; Male; Mem

2021
Riluzole Serum Concentration in Pediatric Patients Treated for Obsessive-Compulsive Disorder.
    Journal of clinical psychopharmacology, 2017, Volume: 37, Issue:6

    Topics: Adolescent; Child; Excitatory Amino Acid Antagonists; Female; Follow-Up Studies; Humans; Male; Obses

2017
No effect of riluzole and memantine on learning deficit following quinpirole sensitization - An animal model of obsessive-compulsive disorder.
    Physiology & behavior, 2019, 05-15, Volume: 204

    Topics: Animals; Behavior, Animal; Cognition; Disease Models, Animal; Dopamine Agonists; Excitatory Amino Ac

2019
The effect of riluzole augmentation in a patient with treatment-resistant obsessive-compulsive disorder, taking two other glutaminergic agents.
    The Journal of neuropsychiatry and clinical neurosciences, 2011,Spring, Volume: 23, Issue:2

    Topics: Adult; Clonazepam; Drug Therapy, Combination; Excitatory Amino Acid Antagonists; Fructose; GABA Modu

2011
Beneficial effects of the antiglutamatergic agent riluzole in a patient diagnosed with obsessive-compulsive disorder and major depressive disorder.
    Psychopharmacology, 2003, Volume: 167, Issue:2

    Topics: Antidepressive Agents; Depressive Disorder, Major; Humans; Male; Middle Aged; Obsessive-Compulsive D

2003
Beneficial effects of the antiglutamatergic agent riluzole in a patient diagnosed with obsessive-compulsive disorder and major depressive disorder.
    Psychopharmacology, 2003, Volume: 167, Issue:2

    Topics: Antidepressive Agents; Depressive Disorder, Major; Humans; Male; Middle Aged; Obsessive-Compulsive D

2003
Beneficial effects of the antiglutamatergic agent riluzole in a patient diagnosed with obsessive-compulsive disorder and major depressive disorder.
    Psychopharmacology, 2003, Volume: 167, Issue:2

    Topics: Antidepressive Agents; Depressive Disorder, Major; Humans; Male; Middle Aged; Obsessive-Compulsive D

2003
Beneficial effects of the antiglutamatergic agent riluzole in a patient diagnosed with obsessive-compulsive disorder and major depressive disorder.
    Psychopharmacology, 2003, Volume: 167, Issue:2

    Topics: Antidepressive Agents; Depressive Disorder, Major; Humans; Male; Middle Aged; Obsessive-Compulsive D

2003
Beneficial effects of the glutamate-modulating agent riluzole on disordered eating and pathological skin-picking behaviors.
    Journal of clinical psychopharmacology, 2006, Volume: 26, Issue:6

    Topics: Depressive Disorder, Major; Excitatory Amino Acid Antagonists; Feeding and Eating Disorders; Female;

2006
Effects of glutamate-related drugs on marble-burying behavior in mice: implications for obsessive-compulsive disorder.
    European journal of pharmacology, 2008, May-31, Volume: 586, Issue:1-3

    Topics: Acoustic Stimulation; Amantadine; Animals; Behavior, Animal; Dizocilpine Maleate; Excitatory Amino A

2008
Riluzole augmentation in treatment-refractory obsessive-compulsive disorder: a series of 13 cases, with long-term follow-up.
    Journal of clinical psychopharmacology, 2008, Volume: 28, Issue:3

    Topics: Adult; Anticonvulsants; Comorbidity; Dose-Response Relationship, Drug; Drug Therapy, Combination; Ex

2008