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OpenTrials
Completed

NCT Number: NCT00405535

Adjunctive Glycine for Obsessive Compulsive Disorder

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Nathan Kline Institute for Psychiatric Research

Orangeburg, New York, 10962, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Glycine

Drug

Placebo

Other

Primary outcomes

  1. Y-BOCS (Yale-Brown Obsessive Compulsive Scale)

    Time frame: 12 weeks after baseline

Secondary outcomes

  1. NIMC-OC scale

    Time frame: 12 weeks after baseline

  2. CGI-Improvement

    Time frame: 12 weeks after baseline

  3. QLS(Quality of Life Scale)

    Time frame: 12 weeks after baseline

  4. Sheehan Disability Scale

    Time frame: 12 weeks after baseline

Sponsors and collaborators

Lead sponsor

Nathan Kline Institute for Psychiatric Research

Other

Collaborators

  • Obsessive Compulsive Foundation

Registry information

Important dates

Study start
2004
Study completion
2006
First posted
Nov 30, 2006
Registry last updated
Dec 16, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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