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Ensayo clínico

At-Home COVID-19 Antibody Test Usability Assessment & Behavior Change Study

NCT: NCT04393961 · WITHDRAWN

ID NCTNCT04393961
EstadoWITHDRAWN
Fecha de inicio2020-04-05
Finalización2020-08-29
SponsorProofPilot (INDUSTRY)
First posted
Last updated

Resumen breve

Radish Health and ProofPilot in coordination with Sanesco are running this study to help establish whether the Premier Biotech COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma Authorized for distribution under emergency use authorization - though not yet FDA reviewed) can be conducted effectively at home to detect COVID-19 antibodies among individuals who have tested positive, or suspect they have previous contracted from COVID-19 and recovered. The study also aims to examine how the results of those tests change social-distancing behaviors and general anxiety over 8 weeks post-test.

Fuente oficial

Ver en ClinicalTrials.gov →

Datos obtenidos de la API de ClinicalTrials.gov. Para conocer el estado más reciente, consulte el registro oficial.

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