Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 3

NCT ID: NCT00000354

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

PHASE1

Study Classification

INTERVENTIONAL

Study Start Date

1996-07-31

Study Completion Date

1997-12-31

Brief Summary

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The purpose of this study is to determine the safety of lofexidine in the treatment of opiate withdrawal. Preliminary data will also be obtained to assess the ability of lofexidine to alleviate opiate withdrawal signs and symptoms.

Detailed Description

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Conditions

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Opioid-Related Disorders Substance-Related Disorders

Study Design

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Primary Study Purpose

TREATMENT

Interventions

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Lofexidine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

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Minimum Eligible Age

21 Years

Maximum Eligible Age

59 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Pennsylvania

OTHER

Sponsor Role collaborator

National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role lead

Principal Investigators

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Charles O'Brien, M.D., Ph.D.

Role: PRINCIPAL_INVESTIGATOR

PDVAMC Treatment Research Center

Locations

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University of Pennsylvania

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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Y01-3-0012-3

Identifier Type: -

Identifier Source: secondary_id

NIDA-3-0012-3

Identifier Type: -

Identifier Source: org_study_id

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