Clinical Trials Directory

Trials / Completed

CompletedNCT04626271

Evaluation of the Accuracy and Usability of the ACR | U.S. Urine Analysis Test System in the Lay User Hands

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
250 (actual)
Sponsor
Healthy.io Ltd. · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

Eligible subjects meeting the pathological profile will be recruited at the designated site by the study personnel. Following subject consent, the subjects will be evaluated for eligibility based on their health condition and history. The ACR \| U.S. kit, in its original packaging, along with the ACR \| U.S. smartphone application will be provided to the subject in a simulated home- use environment. All subjects will be provided with a list of tasks to complete, including providing a urine sample and operating the ACR \| U.S. device on 2 mobile phones. After completing the test, the lay user will complete a post-test questionnaire. The study observer will also complete a questionnaire to collect information regarding the lay users' use of the ACR \| U.S. The device use will be compared with identified risks to determine if the percentage of failures is acceptable. Additionally, measurable usability criteria for specific, critical steps will be evaluated. Following the usability test performed by the lay user, the subjects' urine samples will be tested by the study staff using the comparator device. These results will be considered as the "true value".

Conditions

Interventions

TypeNameDescription
DEVICEACR | U.S. Urine Analysis Test SystemEach study participant will test their urine sample using the ACR \| U.S. test device - a home-use device intended for the semi-quantitative measurement of ACR in the urine (albumin and creatinine ratio) and used to aid in the management of kidney health.
DEVICEURiSCAN Optima Urine AnalyzerUpon completion of the test using the ACR \| U.S. device, each urine sample will be provided to a professional user for further urine analysis test using the comparator device, the URiSCAN Optima Urine Analyzer.

Timeline

Start date
2020-08-31
Primary completion
2020-10-23
Completion
2020-10-25
First posted
2020-11-12
Last updated
2023-05-09
Results posted
2023-05-09

Locations

2 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04626271. Inclusion in this directory is not an endorsement.