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Effects of Buprenorphine and Naloxone in Opiate Addicts - 4

Primary Purpose

Opioid-Related Disorders, Substance-Related Disorders

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Buprenorphine
Sponsored by
National Institute on Drug Abuse (NIDA)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid-Related Disorders focused on measuring opiate dependence

Eligibility Criteria

21 Years - 59 Years (Adult)All SexesDoes not accept healthy volunteers

Please contact site for information.

Sites / Locations

  • University of Pennsylvania

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
September 20, 1999
Last Updated
January 11, 2017
Sponsor
National Institute on Drug Abuse (NIDA)
Collaborators
University of Pennsylvania
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1. Study Identification

Unique Protocol Identification Number
NCT00000355
Brief Title
Effects of Buprenorphine and Naloxone in Opiate Addicts - 4
Official Title
Effects of Buprenophine and Naloxone in Opiate Addicts
Study Type
Interventional

2. Study Status

Record Verification Date
May 1995
Overall Recruitment Status
Completed
Study Start Date
November 1994 (undefined)
Primary Completion Date
January 1996 (Actual)
Study Completion Date
March 1996 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute on Drug Abuse (NIDA)
Collaborators
University of Pennsylvania

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate the behavioral and physiological effects of buprenorphine and naloxone, both alone and in combination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid-Related Disorders, Substance-Related Disorders
Keywords
opiate dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Enrollment
0 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Buprenorphine

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Please contact site for information.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles O'Brien, M.D., Ph.D.
Organizational Affiliation
PDVAMC Treatment Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104 6178
Country
United States

12. IPD Sharing Statement

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Effects of Buprenorphine and Naloxone in Opiate Addicts - 4

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