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Trial of Buprenorphine/Naloxone for Treatment of Opiate Dependence - 9



Trial of Buprenorphine/Naloxone for Treatment of Opiate Dependence - 9

For Condition: Opioid-Related Disorders
Status: No longer recruiting
Sponsor(s): National Institute on Drug Abuse (NIDA) ,
Synopsis: To determine the efficacy and safety of a buprenorphine/naloxone sublingual tablet formulation as an office-based therapy for opiate-dependence treatment.
Details:
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. Meet DSM-IV criteria for opiate dependence. Agree to conditions of the study and sign informed consent. Exclusion Criteria: Psychiatric disorder that requires medication therapy. History of seizures. Pregnant and/or nuring women. Dependence on ETOH or benzodiazepines or other sedative/hypnotics. Acute hepatitis. Other medical condtions that deem participation to be unsafe.
Total Enrollment: 40

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-3-0010-9; 
Study Start Date: 
Record last reviewed: December 2002
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000344

Other Opioid-Related Disorders Studies:
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2. Effects of Alcohol History on Effects of Nitrous Oxide - 9

3. HIV Counseling Intervention for Methadone-Maintained Patients - 2

4. Buprenorphine Maintenance Protocol - 1

5. Buprenorphine Formulation Comparison: Sublingual Tablet vs. Solution - 1

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