Healthy Clinical Trial - Validation of Point of Care Liver Function Tests

Status Terminated

Clinical Trial Summary

This study is testing the accuracy of a point of care device that tests liver function within 20 minutes. The target population will be any adult who had liver function tests ordered and to be drawn on the same day as enrollment.

Clinical Trial Description

Outpatient diagnostics are slow and expensive due to turnaround times, complex workflows and high cost. Sometimes patients do not make it to laboratory testing if a lab is not available on site. Delays in testing can affect medical outcomes or patients can be lost to follow up. Group K developed a paper microfluidic platform with an accompanying mobile application(app). The paper microfluidic device is a simple, inexpensive wax backed device with three testing areas. These areas have a mix of dried proprietary reagents that when combined with a patients drop of blood, or in the future, saliva or urine, will produce results in a color change. An app is then used to interpret the color change and output results to a doctor. The target population is adults who have an indication to collect a liver function panel that will be drawn on the same day as their clinic visit or during their inpatient hospital ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03800069
Study type	Observational
Source	University of Pennsylvania
Contact
Status	Terminated
Phase
Start date	December 3, 2018
Completion date	May 30, 2019

View Details

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