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Alternate-Day Buprenorphine. Phase V - 6



Alternate-Day Buprenorphine. Phase V - 6

For Condition: Opioid-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) , University of Vermont
Synopsis: 72-hour buprenorphine dosing. Buprenorphine blockade challenge.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Double-Blind, Placebo Control, Crossover Assignment
Minimum Age/Maximum Age: 30 Years/49 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-06969-6;  R01-06969-6
Study Start Date: February 1993
Record last reviewed: April 1996
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000224

Other Opioid-Related Disorders Studies:
1. Buprenorphine/Naloxone Treatment for Opiod Dependence-Experiment II-2 - 5

2. Combining Behavioral Treatment with Agonist Maintenance - 1

3. Alternate Day Buprenorphine Administration, Phase XI - 16

4. Multicenter Clinical Trial of Buprenorphine - 3

5. Isoflurane at Subanesthetic Concentrations - 6

Related Studies:

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

Alternate-Day Buprenorphine. Phase V - 6

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