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Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment II-3 - 6

Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment II-3

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00000331
Enrollment
0
Registered
1999-09-21
Start date
2002-12-31
Completion date
2002-12-31
Last updated
2017-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heroin Dependence, Opioid-Related Disorders

Keywords

Heroin Dependence

Brief summary

The purpose of this study is to assess the abuse liability and examine the reinforcing effects of intravenous buprenorphine and buprenorphine/naloxone combinations in healthy, non-drug dependent volunteers.

Detailed description

not available at this time

Interventions

DRUGPlacebo Drug

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
University of Colorado, Denver
Lead SponsorOTHER

Study design

Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Individuals must be healthy, non-drug dependent volunteers, be at least 18 years of age, and have no prior history of drug or alcohol abuse or dependence. Subjects must have had some minimal experience with opioids (e.g. at least two prior exposures)

Exclusion criteria

Individuals with evidence of an active Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) Axis I psychiatric disorder (e.g. psychosis, manic-depressive illness, organic psychiatric disorders), significant medical illness (e.g., liver or cardiovascular disease) or pregnant female subjects are excluded from study participation.

Design outcomes

Primary

MeasureTime frame
Observed withdrawal rating
Pupil diameter
Drug effect characteristics

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026