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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ziminski, JJ | 1 |
Koya, E | 1 |
Pollack, MH | 1 |
Zarate, CA | 1 |
Payne, JL | 1 |
Quiroz, J | 1 |
Sporn, J | 1 |
Denicoff, KK | 1 |
Luckenbaugh, D | 1 |
Charney, DS | 1 |
Manji, HK | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
An Investigation of the Efficacy in Childhood Obsessive-Compulsive Disorder of Riluzole: An Antiglutamatergic Agent[NCT00251303] | Phase 2 | 78 participants (Actual) | Interventional | 2005-08-31 | Completed | ||
Efficacy and Tolerability of Riluzole in Treatment Resistant Depression[NCT01204918] | Phase 2 | 104 participants (Actual) | Interventional | 2011-06-30 | Completed | ||
A Double-Blind Placebo Controlled Trial of Riluzole in Bipolar Depression[NCT00376220] | Phase 2 | 94 participants (Actual) | Interventional | 2004-05-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
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
Intervention | units on a scale (Mean) |
---|---|
Riluzole | 21.72 |
Placebo | 23.30 |
(NCT00251303)
Timeframe: 12 weeks
Intervention | participants (Number) |
---|---|
Riluzole | 3 |
Placebo | 4 |
"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)
Intervention | units on a scale (Mean) |
---|---|
Riluzole Addition to SSRI Antidepressant | 3.20 |
Riluzole/Placebo Addition to SSRI Antidepressant | 5.77 |
Placebo Addition to Standard SSRI Antidepressant | 4.83 |
"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)
Intervention | units on a scale (Mean) |
---|---|
Riluzole Addition to SSRI Antidepressant | 4.13 |
Riluzole/Placebo Addition to SSRI Antidepressant | 0.84 |
Placebo Addition to Standard SSRI Antidepressant | 3.87 |
Responders having at least a 50% improvement in MADRS compared to the baseline in the sequential parallel design (NCT01204918)
Timeframe: 8 weeks therapy
Intervention | Participants (Count of Participants) |
---|---|
Riluzole Addition to SSRI Antidepressant | 6 |
Riluzole/Placebo Addition to SSRI Antidepressant | 8 |
Placebo Addition to Standard SSRI Antidepressant | 10 |
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
Intervention | participants (Number) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Trouble Sleeping | Nightmares | Drowsy | Nervousness | Fatigue | Irratibility | Poor Memory | Poor Concentration | Strange Feeling/Unreal | Hearing/Seeing Things | Abnormal Sensation | Numbness/Tingling | Dizziness | Headache | Blurred Vision | Ringing Ears | Stuffy Nose | Dry mouth | Drooling/Salivation | Muscle Cramp | Muscle Twitch | Trouble Sitting | Tremors/Shakiness | Poor Coordination | Slurred Speech | Rapid Heartbeat | Hyperventilation | Chest Pain | Nausea/Vomiting | Stomach Discomfort | Constipation | Diarrhea | Difficulty Urinating | Frequent Urination | Menstrual Irregularities | Loss of Sexual Interest | Sexual Performance Problems | Delayed/Absent Orgasm | Sweating Excessively | Fluid Retention | Decreased Appetite | Increased Appetite | Weight Gain | Weight Loss | Skin Rash | Diminished Mental Acuity | Difficulty Finding Words | Apathy Emotional Indifference | Dizzy When Standing Up | Bruising | Hair Thinning | Hot Flashes | Clenching Teeth | Strange Taste in Mouth | Unable to Sit Still | |
Placebo Addition to Standard SSRI Antidepressant | 21 | 11 | 22 | 14 | 28 | 23 | 24 | 25 | 5 | 1 | 3 | 4 | 4 | 13 | 5 | 8 | 10 | 10 | 0 | 12 | 6 | 14 | 6 | 5 | 3 | 9 | 3 | 2 | 3 | 9 | 10 | 11 | 1 | 6 | 1 | 22 | 16 | 16 | 14 | 8 | 8 | 15 | 15 | 7 | 3 | 22 | 18 | 21 | 2 | 2 | 8 | 12 | 7 | 5 | 14 |
Riluzole Addition to SSRI Antidepressant | 17 | 9 | 14 | 13 | 14 | 15 | 16 | 16 | 4 | 1 | 3 | 2 | 7 | 8 | 5 | 4 | 5 | 3 | 2 | 5 | 7 | 9 | 8 | 6 | 1 | 8 | 6 | 4 | 3 | 5 | 3 | 2 | 4 | 7 | 0 | 13 | 12 | 9 | 9 | 4 | 5 | 8 | 7 | 5 | 3 | 16 | 15 | 11 | 8 | 4 | 2 | 2 | 4 | 3 | 9 |
Riluzole/Placebo Addition to SSRI Antidepressant | 24 | 15 | 25 | 19 | 26 | 22 | 23 | 28 | 7 | 2 | 5 | 8 | 10 | 14 | 8 | 9 | 14 | 10 | 4 | 16 | 10 | 16 | 9 | 11 | 5 | 13 | 7 | 6 | 5 | 12 | 5 | 7 | 6 | 10 | 2 | 26 | 20 | 19 | 10 | 6 | 7 | 8 | 8 | 7 | 4 | 22 | 21 | 18 | 10 | 2 | 6 | 7 | 13 | 8 | 17 |
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
Intervention | units on a scale (Mean) | |
---|---|---|
Baseline MADRS | Week 8 | |
Active Treatment Group | 32.4 | 21.7 |
Inactive/Placebo Group | 30.4 | 19.0 |
1 review available for riluzole and Recrudescence
Article | Year |
---|---|
Refractory generalized anxiety disorder.
Topics: Anti-Anxiety Agents; Anticonvulsants; Antidepressive Agents, Tricyclic; Antipsychotic Agents; Anxiet | 2009 |
1 trial available for riluzole and Recrudescence
Article | Year |
---|---|
An open-label trial of riluzole in patients with treatment-resistant major depression.
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.
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.
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.
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.
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.
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.
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.
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.
Topics: Adolescent; Adult; Aged; Anticonvulsants; Depressive Disorder, Major; Drug Resistance; Female; Human | 2004 |
1 other study available for riluzole and Recrudescence
Article | Year |
---|---|
Reversing Cocaine-Induced Adaptations and Reducing Relapse: An Opportunity for Repurposing Riluzole.
Topics: Cocaine; Cocaine-Related Disorders; Excitatory Amino Acid Antagonists; Humans; Recurrence; Riluzole | 2018 |