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Alternate Day Buprenorphine Administration, Phase XII - 17



Alternate Day Buprenorphine Administration, Phase XII - 17

For Condition: Opioid-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) , University of Vermont
Synopsis: To determine if six times daily buprenorphine dose is effective in achieving 120 hour buprenorphine dosing.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Placebo Control, Crossover Assignment
Minimum Age/Maximum Age: 18 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-06969-17;  R01-06969-17
Study Start Date: 
Record last reviewed: December 2002
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000235

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2. Neurobiology of Opioid Dependence: 5 - 5

3. Alternate Day Buprenorphine Administration, Phase XI - 16

4. Alternate-Day Buprenorphine. Phase V - 6

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

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Alternate Day Buprenorphine Administration, Phase XII - 17

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