MedPath

A Pilot Trial of Dextroamphetamine for Methamphetamine Dependence

Phase 2
Completed
Conditions
Methamphetamine Addiction
Interventions
Registration Number
NCT00630682
Lead Sponsor
California Pacific Medical Center Research Institute
Brief Summary

The purpose of this study is to assess the safety and effectiveness dextroamphetamine to help methamphetamine users quit or cut down on their use. The study lasts for 9 weeks. Eligible participants will attend research visits twice per week, and will receive individual counseling sessions once per week for all 9 weeks. 50% of the participants will receive the active medication while the other 50% will receive the placebo (sugar pill). Neither the participant or the study team will know if the participant is receiving the placebo or active drug.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • 18-50 yrs. old
Exclusion Criteria
  • pregnant or lactating females

    • Contact site for additional information

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboPlacebo of drug
DextroamphetamineDextroamphetamineActive drug
Primary Outcome Measures
NameTimeMethod
Subjects treated with dextroamphetamine will have better outcomes than subjects treated with placebo, as indicated by the number of urine samples that do not indicate new use of MA (the primary outcome measure)Twice per week for 8 weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CPMC-St. Luke's Campus-Addiction Pharmacology Research Laboratory

🇺🇸

San Francisco, California, United States

© Copyright 2025. All Rights Reserved by MedPath