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Dermatillomania clinical trials

View clinical trials related to Dermatillomania.

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NCT ID: NCT05545891 Not yet recruiting - Clinical trials for Trichotillomania (Hair-Pulling Disorder)

Aripiprazole in Body Focused Repetitive Behaviors

Start date: December 2023
Phase: Phase 2
Study type: Interventional

This study is 6 weeks long and involves subjects taking aripiprazole or placebo. If they are randomly assigned to the aripiprazole arm and are eligible to participate in the study, they will begin by taking 5mg once daily of aripiprazole for two weeks, then 10mg once daily for the remaining three weeks. Efficacy and safety measures will be performed at each visit. Participants will be randomized to receive either aripiprazole or placebo on a 1:1 basis. This blinding will be maintained by the IDS pharmacy at the University of Chicago.

NCT ID: NCT04792645 Completed - Clinical trials for Trichotillomania (Hair-Pulling Disorder)

Memantine in Body Focused Repetitive Behaviors

Start date: June 15, 2021
Phase: Phase 2
Study type: Interventional

This study is 8 weeks long and involves subjects taking memantine or placebo. If they are randomly assigned to the memantine arm and are eligible to participate in the study, they will begin by taking 10mg once daily of memantine for two weeks, then 20mg for the remaining six weeks. Efficacy and safety measures will be performed at each visit. Participants will be randomized to receive either memantine or placebo on a 1:1 basis. This blinding will be maintained by the IDS pharmacy at the University of Chicago.

NCT ID: NCT01063348 Completed - Dermatillomania Clinical Trials

N-Acetyl Cysteine in Pathologic Skin Picking

Start date: September 2012
Phase: Phase 2
Study type: Interventional

The goal of the proposed study is to evaluate the comparative efficacy of N-acetyl cysteine to placebo in pathologic skin picking. Thirty subjects with pathologic skin picking will receive 12 weeks of double-blind treatment with N-acetyl cysteine or matching placebo. The hypothesis to be tested is that N-acetyl cysteine will be more effective than placebo in patients with pathologic skin picking. The proposed study will provide needed data on the treatment of an often disabling disorder that currently lacks a clearly effective treatment.

NCT ID: NCT00513019 Completed - Dermatillomania Clinical Trials

Double-Blind Lamictal (Lamotrigine) in Neurotic Excoriation

Start date: August 2007
Phase: Phase 2
Study type: Interventional

The goal of the proposed study is to evaluate the comparative efficacy of Lamictal (lamotrigine) to placebo in neurotic excoriation. Thirty subjects with neurotic excoriation will receive 12 weeks of double-blind treatment with Lamictal (lamotrigine) or matching placebo. The hypothesis to be tested is that Lamictal (lamotrigine) will be more effective than placebo in patients with neurotic excoriation. The proposed study will provide needed data on the treatment of a disabling disorder that currently lacks a clearly effective treatment.