Technical Accuracy and Userfriendliness of a Point-Of-Care C Reactive Protein Device in a Nursing Home Setting
NCT ID: NCT02104999
Last Updated: 2015-02-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
99 participants
INTERVENTIONAL
2014-06-30
2014-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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Point-of-care test for CRP
Device: C Reactive Protein (CRP) measurement on capillary blood using a point-of-care test to determine the CRP level in the blood
Point-of-care test for CRP
Device: C Reactive Protein (CRP) measurement on capillary blood using a point-of-care test to determine the CRP level in the blood
Interventions
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Point-of-care test for CRP
Device: C Reactive Protein (CRP) measurement on capillary blood using a point-of-care test to determine the CRP level in the blood
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
65 Years
ALL
Yes
Sponsors
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KU Leuven
OTHER
Responsible Party
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Latour Katrien
Research Assistant
Principal Investigators
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Frank Buntinx, PhD
Role: PRINCIPAL_INVESTIGATOR
KU Leuven
Locations
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Domino vzw
Ghent, Oost-Vlaanderen, Belgium
Countries
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Other Identifiers
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CRP-NH0414
Identifier Type: -
Identifier Source: org_study_id
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