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Pharmacotherapy of Body Dysmorphic Disorder in Adolescents



Pharmacotherapy of Body Dysmorphic Disorder in Adolescents

For Condition: Body Dysmorphic Disorder
Status: Suspended
Sponsor(s): National Institute of Mental Health (NIMH) , Brown University,Mount Sinai Medical Center,University of Cincinnati
Synopsis: This is a study of treatment for body dysmorphic disorder (BDD) in adolescents. People with BDD worry about their appearance, which causes them distress or interference with their functioning. This study is evaluating the effectiveness of the medication fluoxetine (Prozac) vs placebo (sugar pill) in BDD. This is a 12 week study for adolescents, ages 12 to 18. All study participants will receive fluoxetine treatment during the study. Participants are paid for their participation.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 12 Years/18 Years
Genders: Both
Protocol Entry Criteria: INCLUSION CRITERIA: (partial listing) - A diagnosis of DSM-IV BDD variant must be present currently and for at least 6 months prior to study entry EXCLUSION CRITERIA: (partial listing) - Schizophrenia or schizoaffective disorder - Current or lifetime DSM-IV bipolar disorder - History of seizure disorder
Total Enrollment: 100

Location and Contact Information:

Mount Sinai Hospital
New York City,  New York,  10029-6574
United States
 

University of Cincinnati
Cincinnati,  Ohio,  45267
United States
 

Butler Hospital, Brown University School of Medicine
Providence,  Rhode Island,  02906
United States
 


Additional Information:
Study ID Numbers:
  58750; 
Study Start Date: April 1999
Record last reviewed: February 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00029471

Other Body Dysmorphic Disorder Studies:
1. Pharmacotherapy of Body Dysmorphic Disorder in Adolescents

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