Semaglutide (Wegovy) Treatment for Trichotillomania

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorUniversity of Chicago

About this trial

This research study is testing the effectiveness and safety of semaglutide (Wegovy) in people with trichotillomania, also known as hair-pulling disorder.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Men and women age 18-75;

Diagnosis of current trichotillomania based on DSM-5 criteria and confirmed using the clinician-administered MIDI (13);

Hair pulling daily with urges to pull as the trigger in >50% of the episodes of pulling;

Women of childbearing age are required to have a negative result on a beta-human chorionic gonadotropin pregnancy test;

Disqualifiers

Infrequent pulling (i.e. less than daily) or automatic pulling (i.e. no urges to pull);

Unstable medical illness or clinically significant abnormalities on laboratory tests, EKG, or physical examination at screen as determined by the investigator;

History of seizures;

Myocardial infarction within 6 months;

Trial design

Design model

Single group

Treatments tested in this trial

  • Semaglutide

    Drug

    All participants in the study will receive semaglutide (Wegovy).

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: Semaglutide (Wegovy)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

NIMH Trichotillomania Severity Scale

Clinician-rated scale assessing trichotillomania symptom severity over the past week that will be administered at all visits. Total scores range from 0-20. Higher scores indicate greater severity.

Time frame
From screening to 1 week after last dose of study drug

Secondary outcomes

1

Clinical Global Impression-Improvement and Severity Scales

Clinician-administered scale consisting of two reliable and valid 7-item Likert scales used to assess severity and change in clinical symptoms. The CGI-S will be used at screening and the CGI-I will be used at every visit after screening. the CGI-S ranges from 1 = "not ill at all" to 7 = "among the most extremely ill." The CGI-I scale ranges from 1 = "very much improved" to 7 = "very much worse."

Time frame
From screening to 1 week after last dose of study drug
2

Massachusetts General Hospital Hair Pulling Scale

A 7-item self-report measure assessing trichotillomania severity over the past week. Total scores range from 0-28. Greater scores indicate worse symptoms.

Time frame
From screening to 1 week after last dose of study drug

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: