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Multicenter Clinical Trial of Buprenorphine - 3



Multicenter Clinical Trial of Buprenorphine - 3

For Condition: Opioid-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) ,
Synopsis: 1) To test efficacy of 4 doses of buprenorphine. 2) Test the safety of buprenorphine.
Details: 12 different sites for a total of 736 subjects (60 at Pizarro, 70 at West LA Tx center, 15 in the 1 year extension)
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Uncontrolled
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 the 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-06082-3; 
Study Start Date: May 1992
Record last reviewed: June 1993
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000207

Other Opioid-Related Disorders Studies:
1. Combined Buprenorphine and Behavioral Treatment without Contingent Reinforcement - 22

2. Alternate Day Buprenorphine Administration, Phase XI - 16

3. Effects of Alcohol History on Effects of Sevoflurane and Nitrous Oxide - 13

4. Isoflurane at Subanesthetic Concentrations - 6

5. Counseling Conditions for Thrice Weekly Buprenorphine in a Primary Care Clinic - 1

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Multicenter Clinical Trial of Buprenorphine - 3

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