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Rapid Diagnostic Test for COVID-19 Based on Antibody Detection (YCOVID)

C

Corporacion Parc Tauli

Status

Completed

Conditions

Covid-19

Treatments

Diagnostic Test: ELISA and Rapid test to detect antibodies against COVID-19

Study type

Observational

Funder types

Other

Identifiers

NCT04490837
2020/587

Details and patient eligibility

About

Ycovid-19 aims to be a rapid diagnostic test for SARS-CoV-2 infection, which will allow a reliable diagnosis to be made in 10 minutes, and on easy-to-use devices. This test will be developed using innovative technology developed at the Parc Taulí University Hospital, which increases the immunogenicity of SARS-CoV-2 differential antigens. The increased immunogenicity of these antigens will allow to detect, with a high sensitivity and specificity, the antibodies in the serum of patients infected with SARS-CoV-2. This test will serve to confirm dubious results as well as reduce false negatives from the PCR test, which will ultimately help reduce transmission of the infection.

Enrollment

3,500 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Professional from Parc Taulí University Hospital
  • Patients with clinical, radiological and/or PCR COVID-19 positive

Exclusion criteria

  • Patients or professionals who do not sign informed consent

Trial design

3,500 participants in 3 patient groups

COVID-19 positive
Description:
Patients with clinical, radiological and/or PCR positive for COVID-19 infection
Treatment:
Diagnostic Test: ELISA and Rapid test to detect antibodies against COVID-19
Normal
Description:
Normal human serum from blood donnors before COVID-19 pandemia
Treatment:
Diagnostic Test: ELISA and Rapid test to detect antibodies against COVID-19
Pathological controls
Description:
Patients with other positive virological serologies
Treatment:
Diagnostic Test: ELISA and Rapid test to detect antibodies against COVID-19

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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