Marinol in Trichotillomania or Obsessive Compulsive Disorder
Primary Purpose
Trichotillomania, Obsessive Compulsive Disorder
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Dronabinol
Sponsored by
About this trial
This is an interventional treatment trial for Trichotillomania focused on measuring Skin Picking, OCD, Trichotillomania, Pathological Skin Picking
Eligibility Criteria
Inclusion Criteria:
- Age 18-65 years
- Obsessive-compulsive disorder (OCD), Trichotillomania (TTM), or Pathological Skin Picking (PSP) as the primary psychiatric diagnosis
- (If OCD) - Subject reports ≥two failed treatments using selective serotonin reuptake inhibitors (SSRIs) for their OCD
- Women's participation required negative results on a beta-human chorionic gonadotropin pregnancy test and stable use of a medically accepted form of contraception.
- Signed informed consent before entry into the study.
Exclusion Criteria:
- Unstable medical illness or clinically significant abnormalities on laboratory tests or physical examination at screening visit
- Current pregnancy or lactation, or inadequate contraception in women of childbearing potential
- A need for medication other than dronabinol with possible psychotropic effects
- History of hypersensitivity to any cannabinoid or sesame oil
- Lifetime history of bipolar disorder type I or II, dementia, or schizophrenia as determined by the Structured Clinical Interview for DSM-IV
- Current (past 12-months) DSM-IV substance abuse or dependence
- Positive urine drug screen at screening
- Initiation of cognitive behavior therapy within 3 months prior to study baseline
- Baseline score of ≥ 17 on the Hamilton Depression Rating Scale (17-item HDRS
- Suicidality based on clinical interview
- History of head injury or neurological disorder (such as seizures)
Sites / Locations
- Ambulatory Research Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Dronabinol
Arm Description
Dronabinol (Marinol) - 2.5mg-15mg by mouth once a day for twelve-weeks
Outcomes
Primary Outcome Measures
Massachusetts General Hospital Hairpulling Scale (MGH-HPS) Total Score
The MGH-HPS is a 7-item, self-report scale that rates urges to pull hair, actual amount of pulling, perceived control over behavior, and distress associated with hair pulling over the past seven days. Total possible score is a 28 indicating the highest level of severity out of a scale from 0-28.
Secondary Outcome Measures
Full Information
NCT ID
NCT01093976
First Posted
March 24, 2010
Last Updated
February 21, 2023
Sponsor
University of Chicago
1. Study Identification
Unique Protocol Identification Number
NCT01093976
Brief Title
Marinol in Trichotillomania or Obsessive Compulsive Disorder
Official Title
An Open-Label Study of Dronabinol, a Cannabinoid Agonist, for Obsessive Compulsive Disorder and the Obsessive-Compulsive Spectrum Disorders Trichotillomania and Pathological Skin Picking
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
January 2011 (Actual)
Study Completion Date
February 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Chicago
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The goal of the proposed study is to evaluate the efficacy and safety of dronabinol in individuals with obsessive-compulsive disorder (OCD) or the obsessive-compulsive spectrum disorders, trichotillomania (TTM) or pathological skin picking (PSP). Fifteen patients with OCD, TTM, or PSP will receive 12 weeks of open-label treatment with dronabinol. The hypothesis to be tested is that dronabinol will be effective and well tolerated in patients with these disorders. The proposed study will provide needed data on the treatment of a disabling disorder that currently lacks a clearly effective treatment.
Detailed Description
The study consists of twelve weeks of open-label dronabinol. All eligible study subjects will be started on open-label dronabinol 2.5mg/day for 3 weeks. The dose will be increased to 5mg/day at visit 2 (Week 3), to10mg/day at visit 3 (Week 6), and to 15mg/day at Visit 4 (Week 9) unless clinical improvement is attained at a lower dose (clinical improvement will be assessed by the investigator with respect to obsessive thoughts, urges and compulsive behaviors). Subjects will be seen every three weeks during the 12-week, open-label study. All efficacy and safety assessments will be performed at each visit. Subjects who are not compliant with their use of study medication (i.e. failing to take medication for three or more consecutive days) will be discontinued from the study.
Laboratory testing, including liver function tests, a blood chemistry panel, and urine toxicology will be completed for subjects at baseline if in the opinion of the study physician the medical history of the subject warrants such tests for their safety. All females, regardless of age, will undergo a urine pregnancy test at screening and all subjects will be required to do a urine drug screen at the screening visit to test for drugs of abuse.
At study conclusion, subjects will be given the option to continue on medication (via prescription) if covered by insurance, and will then be followed in our clinic or referred to another psychiatrist. All study subjects will be offered follow-up care with CBT and/or medication in our outpatient clinic (if covered by insurance) or be given a list of appropriate referrals in the community.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trichotillomania, Obsessive Compulsive Disorder
Keywords
Skin Picking, OCD, Trichotillomania, Pathological Skin Picking
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
14 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Dronabinol
Arm Type
Experimental
Arm Description
Dronabinol (Marinol) - 2.5mg-15mg by mouth once a day for twelve-weeks
Intervention Type
Drug
Intervention Name(s)
Dronabinol
Other Intervention Name(s)
MARINOL
Intervention Description
2.5mg-15mg by mouth once a day for twelve-weeks
Primary Outcome Measure Information:
Title
Massachusetts General Hospital Hairpulling Scale (MGH-HPS) Total Score
Description
The MGH-HPS is a 7-item, self-report scale that rates urges to pull hair, actual amount of pulling, perceived control over behavior, and distress associated with hair pulling over the past seven days. Total possible score is a 28 indicating the highest level of severity out of a scale from 0-28.
Time Frame
Subjects were followed for their duration of participation in the study (12-weeks)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18-65 years
Obsessive-compulsive disorder (OCD), Trichotillomania (TTM), or Pathological Skin Picking (PSP) as the primary psychiatric diagnosis
(If OCD) - Subject reports ≥two failed treatments using selective serotonin reuptake inhibitors (SSRIs) for their OCD
Women's participation required negative results on a beta-human chorionic gonadotropin pregnancy test and stable use of a medically accepted form of contraception.
Signed informed consent before entry into the study.
Exclusion Criteria:
Unstable medical illness or clinically significant abnormalities on laboratory tests or physical examination at screening visit
Current pregnancy or lactation, or inadequate contraception in women of childbearing potential
A need for medication other than dronabinol with possible psychotropic effects
History of hypersensitivity to any cannabinoid or sesame oil
Lifetime history of bipolar disorder type I or II, dementia, or schizophrenia as determined by the Structured Clinical Interview for DSM-IV
Current (past 12-months) DSM-IV substance abuse or dependence
Positive urine drug screen at screening
Initiation of cognitive behavior therapy within 3 months prior to study baseline
Baseline score of ≥ 17 on the Hamilton Depression Rating Scale (17-item HDRS
Suicidality based on clinical interview
History of head injury or neurological disorder (such as seizures)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jon E Grant, JD, MD, MPH
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ambulatory Research Center
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55454
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
21590520
Citation
Grant JE, Odlaug BL, Chamberlain SR, Kim SW. Dronabinol, a cannabinoid agonist, reduces hair pulling in trichotillomania: a pilot study. Psychopharmacology (Berl). 2011 Dec;218(3):493-502. doi: 10.1007/s00213-011-2347-8. Epub 2011 May 19.
Results Reference
derived
Links:
URL
http://www.impulsecontroldisorders.org/index.html
Description
Impulse Control Disorders Clinic - University of Minnesota
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Marinol in Trichotillomania or Obsessive Compulsive Disorder
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