Clinical Trials Directory

Trials / Completed

CompletedNCT00829634

Steady State Kinetics of l-Methamphetamine and Validation of Sensitivity of Dose Estimation

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
California Pacific Medical Center Research Institute · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The intent of this study is to see if the rate that the body breaks down l-methamphetamine (l-MA) could be used as an accurate estimate for the rate that the body breaks down d-methamphetamine (d-MA). l-MA is sold over the counter as a nasal decongestant where as d-MA is the commonly abused form of methamphetamine.

Detailed description

Subjects will screen at St. Luke's Hospital in San Francisco to determine their eligibility. Once enrolled the study will take two weeks. During the first week subjects attend daily, hour-long outpatient visits at San Francisco General Hospital. At these visits subjects will receive an oral dose of l-methamphetamine, have their vitals read, answer questionnaires and receive a blood draw. During the second week of the study subjects are admitted to San Francisco General Hospital for a week long inpatient stay. During this stay the subject continues to receive l-methamphetamine but also receives three doses of d-methamphetamine on three separate days. In addition the subject receives blood draws, has their urine collected, and answers questionnaires.

Conditions

Interventions

TypeNameDescription
DRUGl-methamphetamine5mg of l-methamphetamine per day throughout the 2 week study
DRUGd-methamphetamine15mg on Study Day 9, 30mg on Study Day 11, 45mg on Study Day 13

Timeline

Start date
2008-10-01
Primary completion
2009-09-01
Completion
2009-09-01
First posted
2009-01-27
Last updated
2013-05-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00829634. Inclusion in this directory is not an endorsement.