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.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Urine Toxicology
Timeframe: 6 weeks to 24 weeks