Clinical Trials Directory

Trials / Completed

CompletedNCT04490837

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

Rapid Diagnostic Test for COVID-19 Based on Antibody Detection

Status
Completed
Phase
Study type
Observational
Enrollment
3,500 (actual)
Sponsor
Corporacion Parc Tauli · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTELISA and Rapid test to detect antibodies against COVID-19Ycovid-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

Timeline

Start date
2020-06-22
Primary completion
2020-07-31
Completion
2020-09-30
First posted
2020-07-29
Last updated
2021-07-29

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT04490837. Inclusion in this directory is not an endorsement.