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NCT01093976 · ClinicalTrials.gov registry record · Phase 2

Marinol in Trichotillomania or Obsessive Compulsive Disorder

A Phase 2 study, sponsored by University of Chicago.

Completed
Registry status
Phase 2
Development phase
14
Enrollment target

NCT01093976: Completed Phase 2 study, sponsored by University of Chicago.

NCT01093976 is a Phase 2 study that has completed, run by University of Chicago. The registered enrollment target is 14 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01093976, a Phase 2 study, has completed, sponsored by University of Chicago.

COMPLETED
Registry status
Phase 2
Development phase
14 participants
Enrollment target

Study 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.

Primary Outcome

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.

Interventions

  • DRUG Dronabinol

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2010-04
Est. Completion 2011-02
Phase Phase 2
University of Chicago

796 total trials

What the finished NCT01093976 record still lists

NCT01093976 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% lower).

The record links to 0 conditions, and to 1 intervention - of which Dronabinol is the first listed.

NCT01093976 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01093976 about?

NCT01093976 is a clinical study titled "Marinol in Trichotillomania or Obsessive Compulsive Disorder". 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 1...

What is the current status of trial NCT01093976?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 14 participants. The study started on 2010-04. Estimated completion is 2011-02.

What interventions are being tested in trial NCT01093976?

The interventions under investigation include: Dronabinol (DRUG).

Who is sponsoring clinical trial NCT01093976?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01093976's enrollment target sits among peer trials

14 1941st of 2000 higher than 54 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01093976, the US trial registry maintained by the National Library of Medicine. NCT01093976 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.