Drug Discrimination in Methadone-Maintained Humans Study 1

NCT00593463 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2011-03-11

No results posted yet for this study

Summary

This study involves giving psychoactive drugs intramuscularly (injected into the muscle of the upper arm or the hip) and/or orally, and measuring the subject's ability to tell the difference between one drug and another, as well as measuring the effects of the drugs on mood, physiology (e.g., heart rate, blood pressure, respiration rate) and behavior. Each subject will receive 2-4 of the listed interventions.

Conditions

  • Drug Dependence

Interventions

DRUG

Cycloserine

Cycloserine: 500, 675, 750 mg oral capsule may possibly be given

DRUG

Diltiazem

Diltiazem: 30, 60, 120 mg oral capsule may possibly be

DRUG

Gabapentin

Gabapentin: 100, 200, 400 mg oral capsule may possibly be given

DRUG

Isradipine

Isradipine: 5, 10 mg oral capsule may possibly be given

DRUG

Naloxone

Naloxone: 0.15 mg/70 kg or 0.2 mg I.M. injection may possibly be given

DRUG

Nifedipine

Nifedipine: 5, 10, 20 mg oral capsule may possibly be given

DRUG

Placebo

Placebo (sugar pill or microcrystalline cellulose): oral capsule may possibly be given

DEVICE

Saline

Saline: I.M. injection may possibly be given

DRUG

Verapamil

Verapamil: 30, 60, 120 mg oral capsule may possibly be given

Sponsors & Collaborators

  • University of Arkansas

    lead OTHER

Principal Investigators

  • Alison Oliveto, PhD · University of Arkansas

Study Design

Allocation
NA
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-09-30
Primary Completion
2010-05-31
Completion
2010-05-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00593463 on ClinicalTrials.gov