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
| Type | Name | Description |
|---|---|---|
| DEVICE | Point-of-Care C Reactive Protein measurement on capillary blood | capillary 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.