U.S., Aug. 12 -- ClinicalTrials.gov registry received information related to the study (NCT07758777) titled 'Usability Evaluation of the Intelligent Fingerprinting Drug Screening System' on July 30.
Brief Summary: This is a prospective performance evaluation of usability of the Intelligent Fingerprinting Drug Screening System, conducted in clinic. The total number of healthy adult subjects (male and female) required for enrollment in this study protocol is 45: 15 operators and 30 donors (ideally two donors assigned to one operator). The total duration of the study, from check-in through the end of the study will be 2-4 hours for each donor subject.
Study Start Date: July 20
Study Type: INTERVENTIONAL
Condition:
Healthy Adult Participan...