Clinical Trials Directory

Trials / Completed

CompletedNCT01667172

Technical Accuracy and Userfriendliness of Two Point-of-care C Reactive Protein Devices in Comparison With Laboratory CRP Testing.

Study of Technical Accuracy and Userfriendliness of Two Point-of-care C Reactive Protein Devices

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
300 (actual)
Sponsor
KU Leuven · Academic / Other
Sex
All
Age
1 Month – 65 Years
Healthy volunteers
Accepted

Summary

Study to test technical accuracy and userfriendliness of two Point-of-care C Reactive Protein devices (POC CRP devices) in comparison with laboratory CRP testing on children and adults. Research questions: 1. Are the POC CRP devices technically accurate? Do the measured values agree with CRP values measured at the clinical laboratory? 2. Are the 2 POC CRP devices equivalent ? 2.1. Are the 2 POC CRP devices equally reliable? 2.1.1. Comparison of 2 measurements in the same patient on 1 device (inter-observer-variability) 2.1.2. Comparison of 2 measurements in the same patient on 2 identical devices (inter-device-variability) 2.2. Are the 2 Point-of-Care CRP devices equally userfriendly in a general practice surgery? (userfriendliness

Conditions

Interventions

TypeNameDescription
DEVICEPoint-of-Care C Reactive Protein measurement on capillary bloodcapillary blood fingerstick method to determine C Reactive Protein level in the blood

Timeline

Start date
2012-04-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2012-08-17
Last updated
2012-08-17

Locations

3 sites across 1 country: Belgium

Source: ClinicalTrials.gov record NCT01667172. Inclusion in this directory is not an endorsement.