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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04412473
Other study ID # 7837
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 30, 2020
Est. completion date June 2021

Study information

Verified date May 2020
Source University Hospital, Strasbourg, France
Contact Vincent CASTELAIN, MD, PhD
Phone 33 3 88 12 82 69
Email Vincent.CASTELAIN@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Current management of VID-19 consists of oxygen support without specific treatment. Hospitalization may suddenly require delayed resuscitation. This evolution corresponds to an atypical acute respiratory distress syndrome (ARDS), the mechanism of which is poorly understood and difficult to predict. The general pathophysiology of ARDS, the vascular tropism of SARS-Cov2, the description of coagulopathy and numerous pulmonary artery thromboses in resuscitation and the encouraging investigation of antithrombotics in general ARDS


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date June 2021
Est. primary completion date June 2021
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Major Subject (=18 years) - Subject hospitalised in HUS or GHRMSA for COVID-19 - The diagnosis COVID-19 confirmed by smear or evoked by CT scan or chest X-ray without a differential diagnosis retained in the medical record - Subjects who, after being informed, do not wish to have their data reused for the purposes of this research Exclusion Criteria: - Subject who expressed opposition to participating in the study - Subject under guardianship or trusteeship - Subject under safeguard of justice - Patient hospitalized in a geriatric service or in a ward not labeled COVID (surgery, oncology,...) or in a short-term hospitalization unit without transfer to another service. - Serious patient on admission to the emergency room and recused from resuscitation.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service Médecine Intensive et Réanimation 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 Respiratory Distress and Antithrombolytic Therapy in Patients with covid19 1 month
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