Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Boston, Massachusetts 02114


Purpose:

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


Study summary:

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.


Criteria:

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 medical disorders that might interfere with escitalopram. - Current major depression or prescribed an antidepressant for major depression within the past 12 months. - More than 1 adequate trial (at least 10 weeks at maximally tolerated dose) with another prior SSRI.


NCT ID:

NCT00115011


Primary Contact:

Principal Investigator
Nancy J Keuthen, Ph.D.
Massachusetts General Hospital


Backup Contact:

N/A


Location Contact:

Boston, Massachusetts 02114
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 11, 2017

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.