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NCT04438941 Clinical Trial

Contribution of a Prone Team in Intensive Care During the Covid-19 Epidemic

Sars-CoV2 Clinical Trial

— COVID-PRONE  

Official title:
Contribution of a Prone Team in Intensive Care During the Covid-19 Epidemic

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04438941
Other study ID # 7911
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 25, 2020
Est. completion date June 20, 2020

Study information
Verified date June 2020
Source University Hospital, Strasbourg, France
Contact Bob HEGER, MD
Phone 33 3.69.55.04.43
Email Bob.Heger@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

SARS-CoV-2 induced by COVID 19, involved the hospitalization of 101,932 patients in France, including 4,007 in intensive care (source: Santé Publique France). Alsace was one of the most affected regions on the metropolitan territory with a large number of patients hospitalized at the University Hospital of Strasbourg.

In view of the seriousness of the epidemic and the rapid arrival of new patients requiring mechanical ventilation, 3 new intensive care units have been created on the NHC site alone, making it possible to accommodate a maximum of 111 patients (compared to 52 during normal periods).

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date June 20, 2020
Est. primary completion date June 20, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Criteria for inclusion :

- Major patient (=18 years old)

- Patient hospitalized in intensive care at the NHC, diagnosed COVID + and requiring a VD session of which at least one is performed by the dedicated team.

- patient who has not expressed, after information, his or her opposition to the re-use of his or her data for the purposes of this research

Exclusion criteria :

- Subject who expressed opposition to participating in the study

- Subject under guardianship, curatorship or safeguarding of justice

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Service d'Anesthésie-Réanimation - Nouvel Hôpital Civil Strasbourg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Analysis of the effect of prone position in patients with covid-19 in intensive care 1 month
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