Pharmacotherapy and Intensive Treatment - 2

NCT ID: NCT00000218

Last Updated: 2017-01-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

353 participants

Study Classification

INTERVENTIONAL

Study Completion Date

2005-06-30

Brief Summary

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The purpose of this study is to evaluate desipramine and carbamazepine in reducing cocaine craving; increase outpatient treatment capacity and evaluate their incidence of psychiatric disorders.

Detailed Description

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Conditions

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Cocaine-Related Disorders Substance-Related Disorders

Study Design

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Primary Study Purpose

TREATMENT

Interventions

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Carbamazepine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

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Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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VA Office of Research and Development

FED

Sponsor Role collaborator

National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role lead

Principal Investigators

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William Haning, M.D.

Role: PRINCIPAL_INVESTIGATOR

University of Kansas

Locations

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University of Kansas

Kansas City, Missouri, United States

Site Status

Countries

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United States

Other Identifiers

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R18-06954-2

Identifier Type: -

Identifier Source: secondary_id

NIDA-06954-2

Identifier Type: -

Identifier Source: org_study_id

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