Escitalopram for the Treatment of Self-Injurious Skin Picking (NCT00115011) | Clinical Trial Compass
CompletedPhase 4
Escitalopram for the Treatment of Self-Injurious Skin Picking
United States30 participantsStarted 2002-09
Plain-language summary
The purpose of this study is to determine the effectiveness of escitalopram in treating self-injurious skin picking.
Who can participate
Age range18 Years – 65 Years
SexALL
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Inclusion Criteria:
* Repetitive skin picking resulting in noticeable tissue damage and associated emotional distress and/or functional impairment.
* Age 18-65 years old.
* Duration of skin picking symptoms ≥ 6 months.
* MGH Skin Picking Scale score ≥ 10.
* Written informed consent.
* Females of childbearing potential must have a negative serum or urinary beta-HCG test and be willing to use acceptable methods of birth control during study tenure.
Exclusion Criteria:
* Pregnant women or females of childbearing potential who do not consent to use of a medically acceptable method of contraception.
* Women who are breastfeeding.
* Subjects who pose a serious suicidal or homicidal risk in the judgment of study investigators.
* Serious or unstable medical illness including cardiovascular, hepatic, renal, respiratory, endocrine, neurologic, or hematologic disease.
* Subjects with a dermatologic disorder that causes pruritis.
* Patients on anticoagulant therapy.
* History of seizure disorder.
* Comorbid bipolar disorder, psychosis, organic mental disorder, borderline personality disorder or developmental disorder. Subjects with obsessive compulsive disorder (with primary symptoms other than compulsive skin picking).
* History of substance dependence. If there is a history of substance abuse, subjects should be in remission for ≥ 6 months.
* Current treatment with cognitive behavioral therapy for skin picking.
* Current use of another SSRI medication.
* Other medications for medica…