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Alternate-Day Buprenorphine Administration. Phase VII - 8

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00000226
First Posted: September 21, 1999
Last Update Posted: December 9, 2005
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
University of Vermont
Information provided by:
National Institute on Drug Abuse (NIDA)
  Purpose
The purpose of this study is 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.

Condition Intervention Phase
Opioid-Related Disorders Drug: Buprenorphine Phase 2

Study Type: Interventional
Study Design: Primary Purpose: Treatment
Official Title: Alternate-Day Buprenorphine Administration. Phase VII

Resource links provided by NLM:


Further study details as provided by National Institute on Drug Abuse (NIDA):

Primary Outcome Measures:
  • Drug use
  • Opioid withdrawal
  • Opioid agonist effects
  • Pupil diameter

Estimated Enrollment: 0
Study Start Date: November 1994
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   21 Years to 48 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria
Please contact site for information.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00000226


Locations
United States, Vermont
Treatment Research Center
Burlington, Vermont, United States, 05401
Sponsors and Collaborators
National Institute on Drug Abuse (NIDA)
University of Vermont
Investigators
Principal Investigator: Warren Bickel, Ph.D. University of Vermont
  More Information

Publications:
Patry, Bicket, Tzanis, Badger (in preparation). Every fourth day dosing with buprenorphine (2) A comparison of four different dosing schedules under open and choice procedures.. Patry, Bickel, Tzanis, Badger (in preparation). Every fourth day dosing with buprenorphine (2) A comparison of four different dosing schedules under open and choice procedures.

ClinicalTrials.gov Identifier: NCT00000226     History of Changes
Other Study ID Numbers: NIDA-06969-8
R01-06969-8
First Submitted: September 20, 1999
First Posted: September 21, 1999
Last Update Posted: December 9, 2005
Last Verified: July 1996

Additional relevant MeSH terms:
Opioid-Related Disorders
Substance-Related Disorders
Chemically-Induced Disorders
Mental Disorders
Buprenorphine
Analgesics, Opioid
Narcotics
Central Nervous System Depressants
Physiological Effects of Drugs
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Narcotic Antagonists