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Alternate-Day Buprenorphine Administration. Phase I - 3



Alternate-Day Buprenorphine Administration. Phase I - 3

For Condition: Opioid-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) , University of Vermont
Synopsis: To determine if two times a subject's daily maintenance dose will hold for 48 hours without changes in agonist and antagonist effects.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Double-Blind, Placebo Control, Crossover Assignment
Minimum Age/Maximum Age: 28 Years/45 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-06969-3;  R01-06969-3
Study Start Date: April 1992
Record last reviewed: November 1993
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000221

Other Opioid-Related Disorders Studies:
1. PK0496 Pharmacokinetics of Buprenorphine - 10

2. Alternate-Day Buprenorphine Administration. Phase VII - 8

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

4. Methadone/Buprenorphine Cross-over Study - 4

5. Buprenorphine Maintenance for Opioid Addicts - 1

Related Studies:

Other Opioid-Related Disorders Clinical Trials
Other Vermont Clinical Trials
Other Burlington Clinical Trials

Alternate-Day Buprenorphine Administration. Phase I - 3

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