Adherence Monitoring For Substance Abuse Clinical Trials

Status Completed

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Medication Adherence

Clinical Trial Details

NCT number	NCT01867476
Study type	Observational
Source	California Pacific Medical Center Research Institute
Contact
Status	Completed
Phase	N/A
Start date	January 2013
Completion date	February 2013

View Details

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