Temporal Discounting Delayed Outcomes on Opioid-Dependent Outpatients

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Study Classification

INTERVENTIONAL

Study Start Date

1997-08-31

Brief Summary

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The purpose of this study is to assess the degree in which opioid-dependent outpatients discount the value of an additional maintenance dose of buprenorphine under differing states of opioid deprivation.

Detailed Description

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Conditions

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Opioid-Related Disorders

Study Design

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Primary Study Purpose

TREATMENT

Interventions

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Buprenorphine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

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Minimum Eligible Age

18 Years

Maximum Eligible Age

47 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Principal Investigators

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Warren Bickel, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

University of Vermont

Locations

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Treatment Research Center

Burlington, Vermont, United States

Site Status

Countries

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United States

Other Identifiers

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R01-06969-20

Identifier Type: -

Identifier Source: secondary_id

NIDA-06969-20