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Buprenorphine Dosing Interval - 5

This study has been completed.
Study NCT00000209.   Last updated on August 16, 2005.   Information provided by National Institute on Drug Abuse (NIDA)

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Descriptive Information Fields
Brief Title  Buprenorphine Dosing Interval - 5
Official Title  Buprenorphine Dosing Interval
Brief Summary

The purpose of this study is to explore the feasibility of extending the dosing interval of well maintained buprenorphine patients to 48 and 72 hours, leading to eventual 3 times/week dosing.

Detailed Description
Study Phase Phase II
Study Type  Interventional
Study Design  Treatment, Single Blind, Placebo Control
Primary Outcome Measure  Drug use
Withdrawal symptoms
Opiate and cocaine craving
Secondary Outcome Measure 
Condition  Opioid-Related Disorders
Intervention  Drug: Buprenorphine
MEDLINE PMIDs
Links
Recruitment Information Fields
Recruitment Status  Completed
Enrollment  0
Start Date  November 1992
Completion Date
Eligibility Criteria 

Inclusion Criteria:

M/F ages 21-50. Opiate dependence according to DSM-IV critera. Self-reported use within the last 30 days. Agreeable to conditions of study and signed informed consent.

Exclusion Criteria:

Psychiatric disorder that requires medication therapy. History of seizures. Pregnant and/or nursing women. Dependence on ETOH or benzodiazepines or other sedative-hynotics. Acute hepatitis. Other medical conditions that deem participation to be unsafe.

Gender Both
Ages 21 Years to 50 Years
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00000209
Organization ID NIDA-06082-5
Secondary IDs †† R18-06082-5
Study Sponsor  National Institute on Drug Abuse (NIDA)
Collaborators ††
Investigators 
Principal Investigator:     Walter Ling, M.D.     Friends Research Institute, Inc.    
Information Provided By National Institute on Drug Abuse (NIDA)
Verification Date September 1994
First Received Date  September 20, 1999
Last Updated Date August 16, 2005

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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