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Technical Accuracy and Userfriendliness of a Point-Of-Care C Reactive Protein Device in a Nursing Home Setting

C

Catholic University (KU) of Leuven

Status

Completed

Conditions

Ill Older Adults
Healthy Older Adults

Treatments

Device: Point-of-care test for CRP

Study type

Interventional

Funder types

Other

Identifiers

NCT02104999
CRP-NH0414

Details and patient eligibility

About

Study to test the technical accuracy and userfriendliness of a Point-of-care C Reactive Protein device (POC CRP device) in comparison with laboratory CRP testing in nursing home residents

Enrollment

99 patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Older (65 years or older) nursing home residents

Exclusion criteria

  • Residents not understanding Dutch

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

99 participants in 1 patient group

Point-of-care test for CRP
Other group
Description:
Device: C Reactive Protein (CRP) measurement on capillary blood using a point-of-care test to determine the CRP level in the blood
Treatment:
Device: Point-of-care test for CRP

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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