Efficacy of Naltrexone Treatment as Augmentation to SSRI in OCD Patients

NCT00234689 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL

Last updated 2008-01-30

No results posted yet for this study

Summary

Assessing the efficacy of Naltrexone as augmentation to SSRI in patients with OCD

Conditions

  • Obsessive Compulsive Disorder

Interventions

DRUG

Naltrexone

Sponsors & Collaborators

  • Sheba Medical Center

    lead OTHER_GOV

Principal Investigators

  • Joseph Zohar, MD · Tel Aviv University

  • Revital Amiaz, MD · Tel Aviv University

Study Design

Allocation
RANDOMIZED
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-01-31
Primary Completion
2004-12-31
Completion
2004-12-31

Countries

  • Israel

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00234689 on ClinicalTrials.gov