Viewing Study NCT04733105



Ignite Creation Date: 2024-05-06 @ 3:43 PM
Last Modification Date: 2024-10-26 @ 1:55 PM
Study NCT ID: NCT04733105
Status: COMPLETED
Last Update Posted: 2021-11-09
First Post: 2021-01-24

Brief Title: Pronostic Value of Type I ANTi-Interferon Antibodies in Patients With COVID-19 Acute Respiratory Failure
Sponsor: Assistance Publique - Hôpitaux de Paris
Organization: Assistance Publique - Hôpitaux de Paris

Study Overview

Official Title: Pronostic Value of Type I ANTi-Interferon Antibodies in Patients With COVID-19 Acute Respiratory Failure a Multicenter Observational Study
Status: COMPLETED
Status Verified Date: 2021-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ANTICOV
Brief Summary: Severe SARS-CoV-2 infections are frequently associated with the acute respiratory distress syndrome ARDS which leads to a mortality of 30-40 An altered type I interferon IFN response has been demonstrated in patients with severe COVID-19 together with a high viral load

The aim of the current work is in a large cohort of patients with severe COVID-19 admitted in the ICU to determine the prevalence of patients with positive anti-IFN antibodies and to determine their outcome as compared to patients having negative anti-IFN antibodies
Detailed Description: Severe SARS-CoV-2 infections are frequently associated with the acute respiratory distress syndrome ARDS which leads to a mortality of 30-40 An altered type I interferon IFN response has been demonstrated in patients with severe COVID-19 together with a high viral load A recent study revealed that 10 of patients admitted in the intensive care unit ICU for severe COVID-19 had positive type I anti-IFN antibodies Such finding has potentially important therapeutic implications as patients having positive anti-IFN antibodies could benefit from targeted interventions including plasmapheresis The aim of the current work is in a large cohort of patients with severe COVID-19 admitted in the ICU to determine the prevalence of patients with positive anti-IFN antibodies and to determine their outcome as compared to patients having negative anti-IFN antibodies

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None