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Substance Dependent Teens - Impact of Treating Depression Study 1 - 1 - Article


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Water-Related Diseases


Clinical Trial: Substance Dependent Teens - Impact of Treating Depression Study 1 - 1

This study is currently recruiting patients.

Sponsored by: National Institute on Drug Abuse (NIDA)
Information provided by: National Institute on Drug Abuse (NIDA)

Purpose

The purpose of this study is to evaluate the impact of treating depression on substance dependent teens.

Condition Treatment or Intervention Phase
Alcohol-Related Disorders
Marijuana Abuse
Substance-Related Disorders
 Drug: Fluoxetine
Phase IV

MedlinePlus related topics:  Drug Abuse;   Marijuana Abuse;   Prescription Drug Abuse

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control

Official Title: Substance Dependent Teens - Impact of Treating Depression Study 1

Further Study Details: 

Expected Total Enrollment:  120

The primary study aim is to determine whether fluoxetine + CBT is a more effective treatment than placebo + CBT for substance outcomes, depression, and behavior problems. The current community standard of care often withholds pharmacotherapy for depression in substance abusing adolescents, since it is often assumed that their depressions may remit with SUD treatment alone. However, this is an untested hypothesis in adolescents and one that we propose to test in the current study.

Eligibility

Ages Eligible for Study:  13 Years   -   19 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Must have DSM IV non bipolar Major Depressive disorder (by clinical interview), DSM IV Conduct Disorder, and Non-Tobacco Substance Disorder.

Exclusion Criteria:

  • History of or current psychosis, history of psychotic depression, bipolar disorder I or II, family history of first degree relative with bipolar I, lifetime history of non-substance induced Mania/Hypomania
  • Unstable chronic or serious medical illness
  • Currently pregnant
  • Take psychotrophic medication, past 2 months: medication or treatment for depression, clinically significant laboratory abnormality

Location and Contact Information

Michelle Lohman, R.N.      (303)315-0709    michelle.lohman@uchsc.edu

Colorado
      University of Colorado Health Sciences Center, Denver,  Colorado,  80206,  United States; Recruiting
Paula Riggs, M.D.  303-315-7652    paula.riggs@uchsc.edu 

Study chairs or principal investigators

Paula Riggs, M.D.,  Principal Investigator,  University of Colorado   

More Information

Study ID Numbers:  NIDA-13176-1; R01-13176-1
Record last reviewed:  May 2003
Last Updated:  February 16, 2005
Record first received:  May 21, 2003
ClinicalTrials.gov Identifier:  NCT00061113
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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