Last reviewed · How we verify

NCT04904510

Evaluation of the INDICAID™ COVID-19 Rapid Antigen Test

Completed Results posted Last updated 15 February 2023
What this trial tests

trial testing INDICAID™ COVID-19 Rapid Antigen Test in Covid19 in 297 participants. Completed in 9 March 2021.

Timeline
20 November 2020
Primary endpoint
9 March 2021
9 March 2021

Quick facts

Lead sponsorUniversity of California, Los Angeles
StatusCompleted
Study typeOBSERVATIONAL
Enrollment297
Start date20 November 2020
Primary completion9 March 2021
Estimated completion9 March 2021
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of California, Los Angeles

Who can join

5 and older, any sex, with Covid19. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Test Concordance Primary · Day 1

The concordance with the INDICAID COVID-19 Rapid Antigen Test with an EUA PCR test

GroupValue95% CI
Sample Collection85.375.6 – 91.6

Sponsor's own description

The INDICAID™ Rapid Antigen Test was used in real-world outbreak testing. The antigen test was used together with PCR testing. This study was designed to evaluate whether the addition of a rapid antigen test decreased time to results in a real-world setting.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Covid19

Currently open trials in the same condition.

Other University of California, Los Angeles trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04904510.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing