Addiction & Pharmacology Research Lab, St. Luke's Hospital
San Francisco, California, 94110, United States
NCT Number: NCT01867476
The purpose of this study is to determine the feasibility and accuracy of an automated adherence monitoring system, and to compare the variance between urine and oral fluid riboflavin levels when specimens are obtained 'as usual' and after a one-hour inter specimen interval.
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Notify Me18 year–60 year
All sexes
Observational
San Francisco, California, 94110, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: + 1, 2, 3, 4, 6 hours post dose
California Pacific Medical Center Research Institute
Other
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