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Clinical Trial Summary

This is a combined retrospective and prospective, longitudinal, observational meta-cohort of individuals who will enter the cohort with and without SARS-CoV-2 infection and at varying stages before and after infection. Individuals with and without SARS-CoV-2 infection and with or without Post-Acute Sequelae of COVID-19 (PASC) symptoms will be followed to identify risk factors and occurrence of PASC. This study will be conducted in the United States and subjects will be recruited through inpatient, outpatient, and community-based settings. Study data including age, demographics, social determinants of health, medical history, vaccination history, details of acute SARS-CoV-2 infection, overall health and physical function, and PASC symptom screen will be reported by subjects or collected from the electronic health record using a case report form at specified intervals. Biologic specimens will be collected at specified intervals, with some tests performed in local clinical laboratories and others performed by centralized research centers or banked in the Biospecimen Repository. Advanced clinical examinations and radiologic examinations will be performed at local study sites with cross-site standardization.


Clinical Trial Description

Ambidirectional longitudinal meta-cohort study (combined retrospective and prospective) with nested case-control studies. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05172024
Study type Observational
Source NYU Langone Health
Contact Leora Horwitz, MD
Phone 1-833-422-6819
Email RECOVER_CSC@nyulangone.org
Status Recruiting
Phase
Start date October 29, 2021
Completion date May 23, 2025

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