Escitalopram for the Treatment of Self-Injurious Skin Picking

Last updated: May 19, 2008
Sponsor: Massachusetts General Hospital
Overall Status: Completed

Phase

4

Condition

Kleptomania

Mood Disorders

Treatment

N/A

Clinical Study ID

NCT00115011
2002-P-000888
LXP-MD-36
1200-211220
  • Ages 18-65
  • All Genders

Study Summary

The purpose of this study is to determine the effectiveness of escitalopram in treating self-injurious skin picking.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Repetitive skin picking resulting in noticeable tissue damage and associated emotionaldistress 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 testand be willing to use acceptable methods of birth control during study tenure.

Exclusion

Exclusion Criteria:

  • Pregnant women or females of childbearing potential who do not consent to use of amedically acceptable method of contraception.

  • Women who are breastfeeding.

  • Subjects who pose a serious suicidal or homicidal risk in the judgment of studyinvestigators.

  • 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 personalitydisorder or developmental disorder. Subjects with obsessive compulsive disorder (withprimary symptoms other than compulsive skin picking).

  • History of substance dependence. If there is a history of substance abuse, subjectsshould be in remission for ≥ 6 months.

  • Current treatment with cognitive behavioral therapy for skin picking.

  • Current use of another SSRI medication.

  • Other medications for medical disorders that might interfere with escitalopram.

  • Current major depression or prescribed an antidepressant for major depression withinthe past 12 months.

  • More than 1 adequate trial (at least 10 weeks at maximally tolerated dose) withanother prior SSRI.

Study Design

Total Participants: 30
Study Start date:
September 01, 2002
Estimated Completion Date:
November 30, 2005

Study Description

Purpose: Self-injurious skin picking is a problem documented to occur in 2 % of dermatology patients (Gupta, Gupta and Haberman, 1986) , and approximately 4% of the general population (Keuthen et al., 2000). It is widely under recognized, with medical sequelae that can include scarring, infections, lesions, and potentially life-threatening outcomes (O'Sullivan et al., 1999). In a prior study, fluoxetine was shown to be superior to placebo in treating self-injurious skin picking in a modest-sized double blind trial (Simeon et al., 1997). Similarly, open-label trials of other SSRIs, including sertraline (Kalivas, Kalivas and Gilman, 1996) and fluvoxamine (Arnold et al., 1999) resulted in reductions in skin-picking behavior. Escitalopram is a new SSRI that may have superior efficacy for the treatment of major depression and fewer side effects than other SSRIs. This study aims to assess the efficacy of escitalopram in patients who suffer from self-injurious skin-picking.

Comparisons: Subjects' initial scores on the CGI, HAM-D, SPTS, SPS, SPIS, BDI, BAI, QLESQ, & BDDQ will be compared to subjects' final scores.

Connect with a study center

  • Massachusetts General Hospital

    Boston, Massachusetts 02114
    United States

    Site Not Available

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