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Pharmacological Intervention Project (fluoxetine)



Pharmacological Intervention Project (fluoxetine)

For Condition: Alcoholism
Status: Recruiting
Sponsor(s): National Institute on Alcohol Abuse and Alcoholism (NIAAA) ,
Synopsis: This is a large scale study involving fluoxetine (Prozac) versus a placebo in the treatment of adolescents with alcohol use disorder and major depression. All individuals will receive treatment for 12 weeks with a followup phase lasting 9 months.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Placebo Control
Minimum Age/Maximum Age: 15 Years/18 Years
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: - Meets criteria for alcohol use disorder and major depressive disorder. Exclusion Criteria: - Meets criteria for bipolar disorder, schizoaffective disorder, or schizophrenia. - Hyper- or hypothyroidism, significant cardiac, neurologic, or renal impairment, and those with significant liver disease. - Receiving antipsychotic or antidepressant medication in the month prior to entering the study. - Use of any illicit substance abuse or dependence other than cannabis abuse (and alcohol abuse). - History of intravenous drug use. - Pregnancy, inability or unwillingness to use contraceptive methods. - Inability to read or understand study forms - Less than 15 years of age or over 18 years of age will be excluded.
Total Enrollment: 106

Location and Contact Information:

Western Psychiatric Institute and Clinic *Recruiting*
Pittsburgh,  Pennsylvania,  15213
United States
Recruiting Dr.  Cornelius 412-578-3424


Additional Information:
Study ID Numbers:
  NIAAACOR13370; 
Study Start Date: 
Record last reviewed: November 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00027378

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