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Alternate-Day Buprenorphine Administration. Phase VII - 8



Alternate-Day Buprenorphine Administration. Phase VII - 8

For Condition: Opioid-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) , University of Vermont
Synopsis: To determine if four times a subjects daily maintenance dose will hold for 96 hours without changes in agonist and antagonist effects under open dosing conditions.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Uncontrolled
Minimum Age/Maximum Age: 21 Years/48 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-06969-8;  R01-06969-8
Study Start Date: November 1994
Record last reviewed: July 1996
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000226

Other Opioid-Related Disorders Studies:
1. Methadone/Buprenorphine Cross-over Study - 4

2. Buprenorphine/Naloxone Treatment for Opiod Dependence-Experiment II-2 - 5

3. Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment 1(1) - 1

4. Gradual vs. Rapid Buprenorphine Detoxification - 2

5. Lack of Acute Tolerance Development to Effects of Nitrous Oxide - 4

Related Studies:

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

Alternate-Day Buprenorphine Administration. Phase VII - 8

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