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Alternate-Day Buprenorphine Administration. Phase IV - 5



Alternate-Day Buprenorphine Administration. Phase IV - 5

For Condition: Opioid-Related Disorders
Status: Completed
Sponsor(s): National Institute on Drug Abuse (NIDA) , University of Vermont
Synopsis: To determine if three times a subject's daily maintenance dose will hold for 72 hours without changes in agonist and antagonist effects.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Double-Blind, Placebo Control, Crossover Assignment
Minimum Age/Maximum Age: 20 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-06969-5;  R01-06969-5
Study Start Date: June 1993
Record last reviewed: September 1994
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000223

Other Opioid-Related Disorders Studies:
1. Neurobiology of Opioid Dependence: 2 - 2

2. Novel Medications for Opiate Detoxification - 4

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

4. Buprenorphine Dose Alteration Study - 1

5. A Phase III Placebo-Controlled, Double-Blind Multi-Site Trial of Lofexidine for Opiate Withdrawal - 1

Related Studies:

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

Alternate-Day Buprenorphine Administration. Phase IV - 5

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