A Randomized, Double-Blind, Placebo-Controlled Trial of Flumazenil for the Treatment of Obsessive Compulsive Disorder (OCD)
Primary Purpose
Obsessive Compulsive Disorder
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Flumazenil
Sponsored by
About this trial
This is an interventional treatment trial for Obsessive Compulsive Disorder focused on measuring OCD
Eligibility Criteria
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.
Sites / Locations
- James G. Sullivan, MD
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Sugar Pill, Placebo
Flumazenil
Arm Description
Outcomes
Primary Outcome Measures
Yale Brown Obsessive Compulsive Score
Secondary Outcome Measures
Safety will be assessed by Adverse Events, Changes in physical exam, laboratory values.
Full Information
NCT ID
NCT00997087
First Posted
October 14, 2009
Last Updated
April 18, 2014
Sponsor
Parkway Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT00997087
Brief Title
A Randomized, Double-Blind, Placebo-Controlled Trial of Flumazenil for the Treatment of Obsessive Compulsive Disorder
Acronym
OCD
Official Title
Phase IIa A Randomized, Double-Blind, Placebo-Controlled Trial of Flumazenil for the Treatment of Obsessive Compulsive Disorder.
Study Type
Interventional
2. Study Status
Record Verification Date
April 2014
Overall Recruitment Status
Terminated
Why Stopped
Study completed and data was inconclusive.
Study Start Date
October 2009 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Parkway Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the efficacy of flumazenil in the outpatient treatment of Obsessive Compulsive Disorder (OCD).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obsessive Compulsive Disorder
Keywords
OCD
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
11 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sugar Pill, Placebo
Arm Type
Placebo Comparator
Arm Title
Flumazenil
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Flumazenil
Intervention Description
Sublingual daily
Primary Outcome Measure Information:
Title
Yale Brown Obsessive Compulsive Score
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Safety will be assessed by Adverse Events, Changes in physical exam, laboratory values.
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James G Sullivan, MD
Organizational Affiliation
Parkway Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
James G. Sullivan, MD
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35215
Country
United States
12. IPD Sharing Statement
Learn more about this trial
A Randomized, Double-Blind, Placebo-Controlled Trial of Flumazenil for the Treatment of Obsessive Compulsive Disorder
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