NCT Number: NCT00040053
Ondansetron for the Treatment of Methamphetamine Dependence - 1
The purpose of this study is to assess ondansetron for the treatment of methamphetamine dependence.
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Conditions
Age range
18 year–99 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
South Bay Treatment Center, Chula Vista, California, United States
About this study
This study was designed to be a preliminary assessment of the efficacy and safety of 3-wide range doses of ondansetron (0.25, 1.0 and 4.0 mg taken orally twice per day) to reduce methamphetamine use in subjects with methamphetamine dependence and to determine the optimal dose of ondansetron.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
18 years of age. Treatment seeking for meth dependence.
Exclusion criteria
Please contact site director for more details.
Treatment and study plan
Primary outcomes
-
Clinicial improvement
Sponsors and collaborators
Lead sponsor
National Institute on Drug Abuse (NIDA)
Nih
Collaborators
- University of Texas
Registry information
Official study title
Double-Blind, Placebo-Controlled, Dose Response Trial of Ondansetron for the Treatment of Methamphetamine Dependence.
Important dates
- Study start
- 2002
- Study completion
- 2004
- First posted
- Jun 18, 2002
- Registry last updated
- Jan 12, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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