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NCT00000354 Clinical Trial

Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 3

Substance-Related Disorders Clinical Trial

Official title:
Safety Evaluation of Lofexidine for Treatment of Opioid Withdrawal

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00000354
Other study ID # NIDA-3-0012-3
Secondary ID Y01-3-0012-3
Status Completed
Phase Phase 1
First received September 20, 1999
Last updated January 11, 2017
Start date July 1996
Est. completion date December 1997

Study information
Verified date July 1996
Source National Institute on Drug Abuse (NIDA)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date December 1997
Est. primary completion date September 1997
Accepts healthy volunteers No
Gender All
Age group 21 Years to 59 Years
Eligibility Please contact site for information.

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Lofexidine

Locations
Country Name City State
United States University of Pennsylvania Philadelphia Pennsylvania

Sponsors (2)
Lead Sponsor Collaborator
National Institute on Drug Abuse (NIDA) University of Pennsylvania

Country where clinical trial is conducted

United States, 

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