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Alternate Day Buprenorphine Administration, Phase XI - 16



Alternate Day Buprenorphine Administration, Phase XI - 16

For Condition: Opioid-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) , University of Vermont
Synopsis: 120 hour buprenorphine administration. Open buprenorphine dosing with dose choice after open exposure.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Placebo Control, Crossover Assignment
Minimum Age/Maximum Age: 25 Years/51 Years
Genders: Both
Protocol Entry Criteria: Please contact site for information.
Total Enrollment: 0

Location and Contact Information:

Overall Study Official:
WarrenBickel,  Principal Investigator,  University of Vermont

Treatment Research Center
Burlington,  Vermont,  5401
United States
 


Additional Information:
Study ID Numbers:
  NIDA-06969-16;  R01-06969-16
Study Start Date: 
Record last reviewed: December 2002
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000234

Other Opioid-Related Disorders Studies:
1. A Laboratory Model for Heroin Abuse Medications - 8

2. Combining Behavioral Treatment with Agonist Maintenance - 1

3. Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment III) - 3

4. Alternate-Day Buprenorphine Administration. Phase VI - 7

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

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Alternate Day Buprenorphine Administration, Phase XI - 16

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