Page last updated: 2024-11-03

riluzole and Recrudescence

riluzole has been researched along with Recrudescence in 3 studies

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

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ziminski, JJ1
Koya, E1
Pollack, MH1
Zarate, CA1
Payne, JL1
Quiroz, J1
Sporn, J1
Denicoff, KK1
Luckenbaugh, D1
Charney, DS1
Manji, HK1

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
An Investigation of the Efficacy in Childhood Obsessive-Compulsive Disorder of Riluzole: An Antiglutamatergic Agent[NCT00251303]Phase 278 participants (Actual)Interventional2005-08-31Completed
Efficacy and Tolerability of Riluzole in Treatment Resistant Depression[NCT01204918]Phase 2104 participants (Actual)Interventional2011-06-30Completed
A Double-Blind Placebo Controlled Trial of Riluzole in Bipolar Depression[NCT00376220]Phase 294 participants (Actual)Interventional2004-05-31Completed
[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

Change in Montgomery and Asberg Depression Rating Scale (MADRS)

"This 10 item instrument is completed by the clinician by using a structured interview and defined anchor points, and aims to quantify the degree of depression over the past 7 days. The MADRS is a widely studied instrument for depression, and its reliability and validity are high. This instrument is administered at every study visit during the double-blind RCT, and at the screening, and baseline. 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" (NCT01204918)
Timeframe: 4 weeks of therapy (baseline to week 4)

Interventionunits on a scale (Mean)
Riluzole Addition to SSRI Antidepressant3.20
Riluzole/Placebo Addition to SSRI Antidepressant5.77
Placebo Addition to Standard SSRI Antidepressant4.83

Change in Montgomery and Asberg Depression Rating Scale (MADRS)

"This 10 item instrument is completed by the clinician by using a structured interview and defined anchor points, and aims to quantify the degree of depression over the past 7 days. The MADRS is a widely studied instrument for depression, and its reliability and validity are high. This instrument is administered at every study visit during the double-blind RCT, and at the screening, and baseline. 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" (NCT01204918)
Timeframe: 4 weeks of therapy (week 4 to week 8)

Interventionunits on a scale (Mean)
Riluzole Addition to SSRI Antidepressant4.13
Riluzole/Placebo Addition to SSRI Antidepressant0.84
Placebo Addition to Standard SSRI Antidepressant3.87

Responders Having at Least a 50% Improvement in MADRS Compared to the Baseline

Responders having at least a 50% improvement in MADRS compared to the baseline in the sequential parallel design (NCT01204918)
Timeframe: 8 weeks therapy

InterventionParticipants (Count of Participants)
Riluzole Addition to SSRI Antidepressant6
Riluzole/Placebo Addition to SSRI Antidepressant8
Placebo Addition to Standard SSRI Antidepressant10

Systematic Assessment for Treatment Emergent Events (SAFTEE-SI)

A commonly used instrument originally developed by NIMH and adapted into a self-report instrument. The version of the scale that we plan to use examines in a systematic fashion all possible treatment-emergent side effects and probes specific adverse symptoms, including suicidal thoughts and behaviors, and self-injurious behavior. Presented below are counts of people that had experienced the event by 8 weeks. (NCT01204918)
Timeframe: 8 weeks

,,
Interventionparticipants (Number)
Trouble SleepingNightmaresDrowsyNervousnessFatigueIrratibilityPoor MemoryPoor ConcentrationStrange Feeling/UnrealHearing/Seeing ThingsAbnormal SensationNumbness/TinglingDizzinessHeadacheBlurred VisionRinging EarsStuffy NoseDry mouthDrooling/SalivationMuscle CrampMuscle TwitchTrouble SittingTremors/ShakinessPoor CoordinationSlurred SpeechRapid HeartbeatHyperventilationChest PainNausea/VomitingStomach DiscomfortConstipationDiarrheaDifficulty UrinatingFrequent UrinationMenstrual IrregularitiesLoss of Sexual InterestSexual Performance ProblemsDelayed/Absent OrgasmSweating ExcessivelyFluid RetentionDecreased AppetiteIncreased AppetiteWeight GainWeight LossSkin RashDiminished Mental AcuityDifficulty Finding WordsApathy Emotional IndifferenceDizzy When Standing UpBruisingHair ThinningHot FlashesClenching TeethStrange Taste in MouthUnable to Sit Still
Placebo Addition to Standard SSRI Antidepressant211122142823242551344135810100126146539323910111612216161488151573221821228127514
Riluzole Addition to SSRI Antidepressant1791413141516164132785453257986186435324701312994587531615118422439
Riluzole/Placebo Addition to SSRI Antidepressant241525192622232872581014891410416101691151376512576102262019106788742221181026713817

Mean Change in the Montgomery-Asberg Depression Rating Scale (MADRS) Total Score From Baseline to the End of 8 Weeks of Therapy.

The Montgomery Asberg Depression Rating Scale measures symptoms of depression (MADRS) is a semi-structured interview rating scale for depression that assesses 10 symptoms. The scale is composed of 10 questions with a fixed 7 point scale (0-6). Total score ranges from 0-60. A higher score indicates more depressive symptoms. MADRS Response will be defined as a > 50% reduction in MADRS score from baseline. (NCT00376220)
Timeframe: 8 weeks

,
Interventionunits on a scale (Mean)
Baseline MADRSWeek 8
Active Treatment Group32.421.7
Inactive/Placebo Group30.419.0

Reviews

1 review available for riluzole and Recrudescence

ArticleYear
Refractory generalized anxiety disorder.
    The Journal of clinical psychiatry, 2009, Volume: 70 Suppl 2

    Topics: Anti-Anxiety Agents; Anticonvulsants; Antidepressive Agents, Tricyclic; Antipsychotic Agents; Anxiet

2009

Trials

1 trial available for riluzole and Recrudescence

ArticleYear
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004
An open-label trial of riluzole in patients with treatment-resistant major depression.
    The American journal of psychiatry, 2004, Volume: 161, Issue:1

    Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human

2004

Other Studies

1 other study available for riluzole and Recrudescence

ArticleYear
Reversing Cocaine-Induced Adaptations and Reducing Relapse: An Opportunity for Repurposing Riluzole.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018, Volume: 43, Issue:6

    Topics: Cocaine; Cocaine-Related Disorders; Excitatory Amino Acid Antagonists; Humans; Recurrence; Riluzole

2018