Opioid-Related Disorders Clinical Trial
Official title:
Alternate-Day Buprenorphine. Phase V
Verified date | April 1996 |
Source | National Institute on Drug Abuse (NIDA) |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
The purpose of this study is to evaluate buprenorphine blockade challenge.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 30 Years to 49 Years |
Eligibility | Please contact site for information. |
Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Treatment Research Center | Burlington | Vermont |
Lead Sponsor | Collaborator |
---|---|
National Institute on Drug Abuse (NIDA) | University of Vermont |
United States,
Bickel, Amass, Badger (in preparation) A double-blind controlled trial of buprenorphine dosing every 72 hours in opioid dependenct humans. Bickel, Amass, Badger (in preparation) A double-blind controlled trial of buprenorphine dosing every 72 hours in opioid dependent humans.
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Drug use | |||
Primary | Opioid withdrawal | |||
Primary | Subjective dose estimate | |||
Primary | Drug effect characteristics: ARCI | |||
Primary | Physiological changes in: pupil diameter | |||
Primary | Physiological changes in: blood pressure | |||
Primary | Physiological changes in: heart rate | |||
Primary | Physiological changes in: respiration | |||
Primary | Physiological changes in: bup plasma levels |
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