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Buprenorphine Maintenance Protocol - 1



Buprenorphine Maintenance Protocol - 1

For Condition: Opioid-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) ,
Synopsis: To compare efficacy of 8 mg/day buprenorphine to two doses methadone (30mg/80mg day).
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Double-Blind, Placebo Control
Minimum Age/Maximum Age: 21 Years/50 Years
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: M/F ages 21-50. Opiate dependence according to DSM-IV criteria. 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
Total Enrollment: 0

Location and Contact Information:

Overall Study Official:
WalterLing,  Principal Investigator,  Friends Research Institute

Friends Research Institute
Los Angeles,  California,  90025
United States
 


Additional Information:
Study ID Numbers:
  NIDA-06082-1; 
Study Start Date: October 1990
Record last reviewed: October 1992
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000205

Other Opioid-Related Disorders Studies:
1. Buprenorphine Maintenance for Opioid Addicts - 1

2. Alternate-Day Buprenorphine Administration. Phase II - 4

3. Reinforcing Effects of Brief Exposures to Nitrous Oxide - 8

4. Buprenorphine Maintenance Protocol - 1

5. Safety Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 3

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