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Qualitative Evaluation of Tear Fluid and Blood for Auto Antibodies Produced in Response to COVID-19

N

Namida Lab

Status

Completed

Conditions

Covid19
SARS-CoV 2 Infection

Treatments

Diagnostic Test: SARS-CoV2 Autoantibody detection

Study type

Observational

Funder types

Industry

Identifiers

NCT04542980
CVDTRS001

Details and patient eligibility

About

This study objective is to collect tear and blood samples from individuals with positive SARS-COV2 diagnosis and test those samples for the presence of various SARS-COV2 viral antigens and autoantibodies.

Enrollment

44 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older Has been tested for SARS-CoV2 and awaiting results Sample collection for SARS-CoV2 testing Tested positive for SARS-CoV2 virus (confirmed by RT-PCR) prior to enrollment

Exclusion criteria

  • Under 18 years of age Concurrent eye infection or trauma unrelated to presence of SARS-CoV2 virus. Advanced COVID-19 state what would preclude safe and feasible sample collection.

Trial design

44 participants in 2 patient groups

SARS-CoV2 Positive
Description:
Tear Samples: Tear samples will be collected from 100 patients who have tested positive for the SARS-CoV2 virus. A total of 100 Blood samples will be drawn using standard phlebotomy techniques for venipuncture from patients who have tested positive for the SARS-CoV2 virus.
Treatment:
Diagnostic Test: SARS-CoV2 Autoantibody detection
Control
Description:
Control tear and serum samples will be selected from Namida Lab's own biorepository.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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