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| Sponsor: | National Institute of Mental Health (NIMH) |
|---|---|
| Information provided by: | National Institutes of Health Clinical Center (CC) |
| ClinicalTrials.gov Identifier: | NCT00251303 |
Purpose
This study will examine the effectiveness of riluzole for treating Obsessive-Compulsive Disorder in Youth, Including those with Autism Spectrum Disorders.
| Condition | Intervention | Phase |
|---|---|---|
|
Obsessive-Compulsive Disorder Autism Spectrum Disorder Autism Asperger Disorder Development Disorder |
Drug: Riluzole |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment, Safety/Efficacy Study |
| Official Title: | An Investigation of the Efficacy in Childhood Obsessive-Compulsive Disorder of Riluzole: An Antiglutamatergic Agent |
| Estimated Enrollment: | 75 |
| Study Start Date: | August 2005 |
| Estimated Study Completion Date: | September 2009 |
| Estimated Primary Completion Date: | September 2009 (Final data collection date for primary outcome measure) |
Obsessive-Compulsive Disorder (OCD) is a chronic psychiatric disorder characterized by the presence of intrusive and unwanted obsessional thoughts and images and of compulsive behaviors. Its presentation during childhood is similar to that seen in adulthood, except that children sometimes lack insight into the senselessness of the thoughts and behaviors. Although many patients benefit from treatment with selective serotonin reuptake inhibitors (SSRIs), a significant proportion have limited or no response to these medications. Additionally, these medicines have been associated with a slight but significant increase in onset of suicidal thoughts among adolescents being treated for depression or OCD. Cognitive behavioral therapy (CBT) may also be effective for OCD, alone or in combination with SSRIs, but there is a shortage of qualified therapists, and many patients and families cannot participate effectively in the therapy. Further, in a recent report on a multi-site study of childhood OCD, CBT alone at one site fared little better than placebo.
There is a pressing need, then, for the development of alternative, novel treatments for pediatric OCD. Neuropsychological and neuroimaging data suggest that OCD may arise from dysfunction of orbitofronto-striato-thalamocortical circuitry. Glutamate plays a crucial role in the regulation of excitatory activity within this circuit and may be involved in the etiopathogenesis of OCD. If so, then agents which reduce glutamatergic neurotransmission may provide unique antiobsessional benefits. Riluzole is a medication that reduces glutamatergic activity. It is currently being studied in adults with OCD, and this two-stage study will evaluate the possibility that riluzole will help children with OCD, Riluzole has been approved by the Food and Drug Administration (FDA) for treatment of amyotrophic lateral sclerosis (ALS), and is currently under investigation at the NIMH for treatment of depression.
The first stage of this investigation has been completed. Six children with OCD, ages 7 to 17 years, received riluzole as part of a study that evaluated the drug's safety and estimated the appropriate dose of riluzole Riluzole was added to the children's current medication regimen or was used as sole agent. The second stage of the investigation will enroll up to 60 additional subjects with OCD including some who have both autistic spectrum disorder (ASD) and OCD. The subjects will participate in a double-blind, placebo-controlled12-week trial of riluzole as a sole agent or as an augmentation to their currently inadequate therapy. Following the double-blind portion of the trial, subjects may receive three months of open-label treatment with riluzole, if it is clinically indicated. All subjects will be followed at regular intervals until one year from baseline.
Eligibility| Ages Eligible for Study: | 7 Years to 17 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Subjects may be included in the study only if they meet all of the following criteria:
EXCLUSION CRITERIA:
Subjects will be excluded from the study for any of the following reasons:
Contacts and Locations| Contact: Lorraine Lougee, L.C.S.W. | (301) 496-5323 | ocdnimh@intra.nimh.nih.gov |
| United States, Maryland | |
| National Institutes of Health Clinical Center, 9000 Rockville Pike | Recruiting |
| Bethesda, Maryland, United States, 20892 | |
More Information
| Responsible Party: | National Institutes of Health ( Paul J. Grant, M.D./National Institute of Mental Health ) |
| Study ID Numbers: | 050225, 05-M-0225 |
| Study First Received: | November 9, 2005 |
| Last Updated: | September 24, 2009 |
| ClinicalTrials.gov Identifier: | NCT00251303 History of Changes |
| Health Authority: | United States: Federal Government |
|
Clinical Trial Glutamate Antagonist Pediatrics Basal Ganglia Neurophyschological |
Obsessive Compulsive Disorder OCD Riluzole Rilutek |
|
Riluzole Neurotransmitter Agents Disease Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Asperger Syndrome Excitatory Amino Acid Agents Protective Agents Neuroprotective Agents Pharmacologic Actions Child Development Disorders, Pervasive |
Pathologic Processes Anxiety Disorders Autistic Disorder Mental Disorders Therapeutic Uses Mental Disorders Diagnosed in Childhood Central Nervous System Agents Anticonvulsants Obsessive-Compulsive Disorder Excitatory Amino Acid Antagonists |