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Substance Abuse Pre-Treatment Screening Study
Sponsor: The University of Texas Health Science Center, Houston
Summary
The overarching goal of this project is to have a consolidated consent and evaluation procedure that will lead potential subjects to the most appropriate clinical trial or human laboratory study (and its consent process) for their presenting concerns or interests. A second purpose is to have a consolidated intake data base on which secondary analyses can be conducted.
Official title: General Evaluation of Eligibility for Substance Abuse/Dependence Research
Key Details
Gender
All
Age Range
18 Years - 60 Years
Study Type
OBSERVATIONAL
Enrollment
7500
Start Date
2005-10
Completion Date
2026-06
Last Updated
2023-12-20
Healthy Volunteers
No
Interventions
modafinil
400 mg daily
d-amphetamine
60mg daily
L-Dopa
800/200mg daily
Naltrexone
50mg daily
Locations (1)
University of Texas Medical School- Houston, Dept. of Psychiatry Mental Sciences Institute
Houston, Texas, United States