C-reactive Protein Levels Among Individuals With COVID-19

NCT ID: NCT04373798

Last Updated: 2021-08-18

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

1006 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-04

Study Completion Date

2021-03-30

Brief Summary

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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.

Detailed Description

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Conditions

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Coronavirus Infection

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Suspected COVID-19

Individuals with symptoms who are seen at covid19 check points for covid19 diagnosis.

C-reactive protein

Intervention Type DIAGNOSTIC_TEST

Measurement of CRP value from blood sample taken at covid19 check point (baseline).

Interventions

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C-reactive protein

Measurement of CRP value from blood sample taken at covid19 check point (baseline).

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Henning Bliddal

OTHER

Sponsor Role lead

Responsible Party

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Henning Bliddal

Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Henning Bliddal, DMSc

Role: PRINCIPAL_INVESTIGATOR

The Parker Institute

Locations

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The Parker Institute, Frederiksberg Hospital

Copenhagen, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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APPI2-CV-2020-02

Identifier Type: -

Identifier Source: org_study_id

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