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Nefazodone in the Treatment of Cocaine Dependence and Depression - 4 - Article


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Male Genital Disorders

Penile Disorders; Testicular Disorders 




Clinical Trial: Nefazodone in the Treatment of Cocaine Dependence and Depression - 4

This study is no longer recruiting patients.

Sponsors and Collaborators: National Institute on Drug Abuse (NIDA)
New York MDRU
Information provided by: National Institute on Drug Abuse (NIDA)

Purpose

The purpose of this study is the use of Nefazodone in the treatment of cocaine dependence and depression comorbidity.

Condition Treatment or Intervention Phase
Cocaine-Related Disorders
Substance-Related Disorders
 Drug: Nefazodone
Phase II

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

Study Type: Interventional
Study Design: Treatment, Placebo Control

Official Title: Efficacy of Nefazodone in Cocaine Dependent Subjects

Further Study Details: 

Study start: February 1997;  Study completion: January 1999

The objective of this study is to determine the safety and efficacy of nefazodone (Serzone ) in depressed cocaine dependent subjects. This is a hypothesis-testing study which will explore whether cocaine usage will be reduced in the nefazodone treatment group compared to a placebo control group.

Eligibility

Ages Eligible for Study:  21 Years   -   55 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

DSM-IV diagnosis of cocaine dependence, Depression score of 12 or above and history of depression. Males and non-pregnant, non-nursing females 21-55 years of age.

Exclusion Criteria:

Axis I diagnosis other than substance use disorder, major depression, anxiety of dysthymic disorder. Physiological dependence on alcohol. Significant medical or neurological history. Abnormal UA, CBC or Chem 23 (LFT's may be up to 3 times normal). Enrollment in an opiate-substitution treatment program within 45 days of enrollment in the present study.


Location Information


New York
      New York MDRU, New York,  New York,  10010,  United States

Study chairs or principal investigators

John Rotrosen, M.D.,  Principal Investigator,  New York MDRU   

More Information

Study ID Numbers:  NIDA-5-0013-4; Y01-5-0013-4
Record last reviewed:  February 1997
Last Updated:  February 16, 2005
Record first received:  April 18, 2001
ClinicalTrials.gov Identifier:  NCT00015210
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


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

Resources



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Page Updated: October 3, 2005
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