Status:
COMPLETED
Study Project Comparing the Sequelae of COVID-19 Infection in Patients Who Have and Have Not Received Ventilatory Support in Critical Care
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Conditions:
Covid19
Eligibility:
All Genders
18+ years
Brief Summary
To assess the proportion of post-intensive care syndrome (PICS) of patients who received high flow humidified oxygen with FiO2 ≥50% for more than 48h and / or who received mechanical ventilation for m...
Eligibility Criteria
Inclusion
- \-
- Group 1: patients hospitalized in intensive care units for ARDS with SARS-CoV-2
- Major
- Admitted between March 1 and May 10, 2020 in one of the sectors of the Bicêtre hospital approved for critical care
- proven SARS-CoV-2 infection
- Treated by invasive mechanical ventilation or high flow humidified oxygen with FiO2 ≥50% for more than 48 hours.
- Group 2: patients hospitalized outside intensive care units
- Major
- Admitted between March 1 and May 10, 2020 in an area of Bicêtre hospital having cared for patients infected with SARS-CoV-2 excluding critical care: pulmonology, internal medicine / orthopedics, infectious diseases, nephrology , acute geriatrics, neurology.
Exclusion
- Patients having refused the post consultation at 3 month
- Without social security coverage
Key Trial Info
Start Date :
June 1 2020
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2020
Estimated Enrollment :
478 Patients enrolled
Trial Details
Trial ID
NCT04704388
Start Date
June 1 2020
End Date
October 1 2020
Last Update
April 1 2021
Active Locations (1)
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1
Bicêtre Hospital
Le Kremlin-Bicêtre, France, 94270