Skip to content

A Randomized, Double-Blind, Placebo-Controlled Trial of Flumazenil for the Treatment of Obsessive Compulsive Disorder

Phase IIa A Randomized, Double-Blind, Placebo-Controlled Trial of Flumazenil for the Treatment of Obsessive Compulsive Disorder.

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00997087
Acronym
OCD
Enrollment
11
Registered
2009-10-16
Start date
2009-10-31
Completion date
2012-12-31
Last updated
2014-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obsessive Compulsive Disorder

Keywords

OCD

Brief summary

The purpose of this study is to evaluate the efficacy of flumazenil in the outpatient treatment of Obsessive Compulsive Disorder (OCD).

Interventions

DRUGFlumazenil

Sublingual daily

Sponsors

Parkway Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
19 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Able to understand and provide written informed consent. * Age 19-60, inclusive. * Diagnosis documented according to DSM-IV of OCD. * Exhibits moderate to severe OCD symptoms and a minimum score of 16 or greater -YBOCS at screening. * Willing and able to discontinue current medications taken for the treatment of OCD. * Able to attend and participate in all study visits. * Agree to continue if in current psychosocial therapy throughout the remainder of the study. * If female and of child-bearing potential, willing to use an acceptable method of birth control for the duration of the study. * If male, willing to use barrier method of birth control or had previous vasectomy.

Exclusion criteria

* Have other DSM-IV Axis I diagnoses. * Pregnant as confirmed by urine analysis, or lactating, or unwilling to comply with use of contraception. * Unwilling or unable to washout (discontinue) from prohibited medications such as antidepressants (See Appendix 2). * Depression symptoms with a score of 15 or greater on the MADRS at screening. * Current suicidal ideation or plan within the last 30 days. * Have a medical condition which, in the opinion of the investigator, makes study participation unsafe or noncompliant. * Abnormal physical exam or laboratory values which, in the opinion of the investigator, makes study participation unsafe or may require introduction of concomitant medications during the course of the study. * Benzodiazepine and/or similar sedative-hypnotic or anxiolytic use or abuse within 15 days of potential flumazenil treatment: patients must not be habituated to benzodiazepines and must provide a urine sample that is negative for benzodiazepines, must not be taking supra-therapeutic doses of zolpidem (AmbienTM) or zaleplon (SonataTM ). (See Appendix 2). * Patients who are taking Phenobarbital for a documented seizure disorder can be admitted. Patients with a seizure disorder being managed with clonazepam (KlonopinTM ) or other benzodiazepine cannot participate, patients must not be taking TCA, lithium, methylxanthines, isoniazid, propoxyphene, monoamine oxidase inhibitors, bupropion HCL, and cyclosporine. (See Appendix 2). * Previously treated with flumazenil for OCD. * AIDS as determined by self-report.

Design outcomes

Primary

MeasureTime frame
Yale Brown Obsessive Compulsive Score12 weeks

Secondary

MeasureTime frame
Safety will be assessed by Adverse Events, Changes in physical exam, laboratory values.12 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026