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CRP-POCT in suspected airway infected patients in the long-term care facility

CRP-POCT in suspected airway infected patients in the long-term care facility - CRP-SAIE (CRP-suspected airway infected elderly)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43304
Enrollment
50
Registered
2017-01-18
Start date
2017-02-15
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pneumonia respiratory tract infection

Interventions

The intervention will consist of one blood test for the patiënt and a questionnaire for the physician.
Aged
C-Reactive Protein
Respiratory Tract Infections

Sponsors

Stichting Opella
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: All institutionalized patiënts with suspected airway infection

Exclusion criteria

Exclusion criteria: Patients, or their first legal representative, who do not sign the informed consent, will be excluded. Also, if the physician wants to give antibiotics nonetheless, patients will be excluded and if a patient doesn*t want to receive antibiotic treatment anymore, exclusion will follow as well. If a patiënt, representative or physician assesses the test as too painful or traumatic for the patient.

Design outcomes

Primary

MeasureTime frame
Main study parameters/endpoints: The main endpoint is a difference in first-consult-prescribed antibiotic use in patients who had a CRP test.

Secondary

MeasureTime frame
- relation between height of CRP and number of antibiotic prescriptions - relation between parameters for illness and number of antibiotic prescriptions - the value of pre-test illness according to the physician.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)