Last updated: November 18, 2020
Sponsor: University of Chicago
Overall Status: Completed
Phase
2
Condition
Alopecia
Hair Loss
Scalp Disorders
Treatment
N/AClinical Study ID
NCT02473913
15-0178
Ages 10-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Males and females ages 10-65.
- Diagnosis of current trichotillomania (TTM) based on DSM-5 criteria and confirmedusing the clinician-administered Structured Clinical Interview for DSM-5 (SCID);
- Hair-pulling behavior within 2 weeks prior to enrollment;
- Child able and willing to provide active assent for participation;
- Legal guardian available to provide consent for participation.
Exclusion
Exclusion Criteria:
- Infrequent hair-pulling (i.e. less than one time per week) that does not meet DSM-5criteria for trichotillomania;
- Unstable medical illness as determined by the investigator;
- History of seizures;
- Current use of stimulants coinciding with onset or exacerbation of trichotillomaniasymptoms or other current medications coinciding with exacerbation or onset ortrichotillomania symptoms;
- Clinically significant suicidality (defined by the Columbia Suicide Severity RatingScale);
- Baseline score of ≥17 on the Hamilton Depression Rating Scale (17-item HDRS);
- Lifetime history of bipolar disorder type I or II, schizophrenia, autism, anypsychotic disorder, or any substance use disorder;
- Initiation of psychotherapy or behavior therapy within 3 months prior to studybaseline;
- Previous treatment with milk thistle;
- Any history of psychiatric hospitalization in the past year.
Study Design
Total Participants: 22
Study Start date:
March 01, 2015
Estimated Completion Date:
September 30, 2020
Study Description
Connect with a study center
University of Chicago
Chicago, Illinois 60637
United StatesSite Not Available

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.