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NCT04636294 Clinical Trial

Borderline COVID-19 PCR Test Result

Covid19 Clinical Trial

Official title:
Follow-up of Patients With a Borderline COVID-19 PCR Test Result

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04636294
Other study ID # f/2020/166
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 1, 2020
Est. completion date February 15, 2021

Study information
Verified date February 2021
Source Jessa Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Follow-up of patients with a borderline PCR result. Data of patients that were re-tested within 96 hours after receiving a borderline COVID-19 PCR result are reviewed. This is a retrospective study.

Recruitment information / eligibility
Status Completed
Enrollment 30000
Est. completion date February 15, 2021
Est. primary completion date February 15, 2021
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Every individual that delivers a nasopharyngeal lysate for SARS-CoV-2 RNA determination by PCR. Exclusion Criteria: - Patients without a previous borderline COVID-19 PCR result within 96 hours are excluded for the follow-up study.

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• SARS-CoV-2 PCR
SARS-CoV-2 PCR of nasopharyngeal lysate.

Locations
Country Name City State
Belgium Clinical Laboratory Jessa Hospital Hasselt Limburg

Sponsors (1)
Lead Sponsor Collaborator
Jessa Hospital

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Ratio of positivity conversion after receiving a COVID-19 borderline PCR result. 3 days
Secondary Symptoms predicting COVID-19 positivity conversion after receiving a borderline PCR result. 1 day
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