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Alternate-Day Buprenorphine Administration. Phase VI - 7



Alternate-Day Buprenorphine Administration. Phase VI - 7

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 subject's daily maintenance dose will hold for 96 hours without changes in agonist and antagonist effects.
Details:
Eligibility:
Study Type:
  Observational, Cross-Sectional
Minimum Age/Maximum Age: 21 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-06969-7;  R01-06969-7
Study Start Date: December 1992
Record last reviewed: December 1996
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000225

Other Opioid-Related Disorders Studies:
1. Pharmacokinetics of LAAM in Methadone Patients - 5

2. Safety Evaluation of Lofexidine for Treatment of Opioid Withdrawal - 7

3. Trial of Buprenorphine/Naloxone for Treatment of Opiate Dependence - 9

4. Buprenorphine Maintenance for Opioid Addicts - 1

5. Combining Behavioral Treatment with Agonist Maintenance - 1

Related Studies:

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

Alternate-Day Buprenorphine Administration. Phase VI - 7

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