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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04373798
Other study ID # APPI2-CV-2020-02
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 4, 2020
Est. completion date March 30, 2021

Study information

Verified date August 2021
Source Frederiksberg University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective of this multi-center study is to clarify the value of a CRP measurement for triage of patients initially presenting with light symptoms of the COVID-19 infection. Current recommendations of management of COVID-19 include large-scale tests for virus. Such tests reveal whether an individual is infected with the virus, however, the demonstration of virus per se has no prognostic value for the ensuing course of the COVID-19 disease. Publications of possible treatments strategies increase exponentially, while evidence of triage of the affected individuals is mainly based on the level of pulmonary affection as measured by the Oxygen saturation. To inform decision making for which patients are to be hospitalized due to risk of developing more severe affection, this study addresses the question, whether triage may be performed with the aid of a simple CRP measurement.


Recruitment information / eligibility

Status Completed
Enrollment 1006
Est. completion date March 30, 2021
Est. primary completion date August 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. A test for COVID-19 taken at the check point 2. Signed, informed consent for blood test to be drawn for the Biobank Exclusion Criteria: 1. Former admission to hospital for COVID-19 2. Direct admission from check point.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
C-reactive protein
Measurement of CRP value from blood sample taken at covid19 check point (baseline).

Locations

Country Name City State
Denmark The Parker Institute, Frederiksberg Hospital Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Henning Bliddal

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hospitalisation Admission to a hospital. Reason for admission is recorded. within 28 days
Secondary Death within 28 days
Secondary Transfer to Intensive Care Unit within 28 days
Secondary Oxygen treatment during hospitalisation within 28 days
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