Official Title
Comparison of the Efficacy of Rapid Tests to Identify COVID-19 Infection (CATCh COVID-19)
Brief Summary

This study is designed to compare the efficacy of detection of COVID-19 infection using the serology test in blood sample and the PCR-based test in the nasopharyngeal (NP) and sputum sample. Furthermore, it aims to evaluate the temporal trend of appearance of IgM and IgG in blood.

Detailed Description

The investigators hypothesize that viral-RNA test using sputum will be equally efficient as
the test performed in NP swab. Moreover, the serology test and the PCR-based test will be
comparable in efficacy for detection of infection

Unknown status
COVID-19

Diagnostic Test: diagnostic tests for COVID-19 infection

Compare the efficacy of diagnostic tests for COVID-19 infection in detecting antibodies and viral-RNA

Eligibility Criteria

Inclusion Criteria:

- • Male or female over 18 years of age at the time of enrollment

- Current symptoms of COVID-19 ; fever alone or fever and at least one of the
following symptoms need to be present

- Dry cough

- Sore throat

- Shortness of breath

- Chills

- Muscle pain

- Headache

- New loss of taste or smell

- Chills with repeated shaking

Exclusion Criteria:

- • Unwilling to provide informed consent

- Unwilling to undergo bi-weekly serological test during the 1-month enrollment

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 85 Years
Countries
United States
Locations

Texas Cardiac Arrhythmia Institute
Austin, Texas, United States

Investigator: Mitra Mohanty, MD
Contact: 512-544-8186
mitra1989@gmail.com

Contacts

MITRA Mohanty, MD
5127842651
mitra1989@gmail.com

Deb Cardinal, RN MBA
512) 807-3150

Texas Cardiac Arrhythmia Research Foundation
NCT Number
MeSH Terms
COVID-19