Adjunctive Glycine for Obsessive Compulsive Disorder
- Conditions
- Obsessive Compulsive Disorder
- Interventions
- Other: placebo
- Registration Number
- NCT00405535
- Lead Sponsor
- Nathan Kline Institute for Psychiatric Research
- Brief Summary
The purpose of this study is to determine whether individuals with obsessive compulsive disorder who will take a preparation of the amino acid glycine in addition to their current treatment, may experience improvement in their symptoms.
- Detailed Description
Individuals with obsessive compulsive disorder (OCD) often find inadequate relief, even with the best of currently available treatments. Some evidence suggests the the neurotransmitter glutamate may be a useful target for new treatments for OCD. The amino acid glycine, if given orally in adequate dosages, can have specific effects on one particular glutamate receptor molecule in the brain, that might be helpful with OC symptoms. This randomized, double-blind protocol will have study participants who suffer with OCD take either a glycine preparation or placebo for 12 weeks. Clinical measures (e.g., Y-BOCS, NIMH-OC) will be recorded at each visit to determine whether those taking the glycine experience clinical benefit.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 24
- Diagnosis of OCD present for at least 1 year
- Male or female, age 18 to 65
- Stable medication regimen for 12 weeks prior to study entry
- at least moderately severe OC symptoms
- Active substance use disorder within the last 6 months
- Comorbid schizophrenia, schizoaffective disorder, bipolar disorder, tic disorder, Tourette Disorder, schizotypal personality disorder
- Hoarding as the principal OCD symptom
- Insulin-dependent diabetes mellitus
- Pregnant or breastfeeding
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description B placebo placebo powder A glycine glycine powder
- Primary Outcome Measures
Name Time Method Y-BOCS (Yale-Brown Obsessive Compulsive Scale) 12 weeks after baseline
- Secondary Outcome Measures
Name Time Method CGI-Improvement 12 weeks after baseline QLS(Quality of Life Scale) 12 weeks after baseline NIMC-OC scale 12 weeks after baseline Sheehan Disability Scale 12 weeks after baseline
Trial Locations
- Locations (1)
The Nathan Kline Institute for Psychiatric Research
🇺🇸Orangeburg, New York, United States