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Clinical Trial Summary

This is a combined retrospective and prospective, longitudinal, observational meta-cohort of individuals age 0-25 years who will enter the cohort with and without SARS-CoV-2 infection at varying stages before and after infection. Individuals with and without SARS-CoV-2 infection and with or without PASC symptoms will be followed to identify risk factors and occurrence of PASC. This study will be conducted in the United States and participants 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 symptoms will be reported by participants 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 NCT05172011
Study type Observational
Source NYU Langone Health
Contact Stuart Katz, MD, MS
Phone 1-833-422-6819
Email Stuart.Katz@nyulangone.org
Status Recruiting
Phase
Start date March 1, 2022
Completion date May 23, 2025

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