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Clinical Trials/NCT04412473
NCT04412473UnknownNot Applicable

COVID-19 Respiratory Distress and Antithrombotic Drugs inSubject's Habits

University Hospital, Strasbourg, France1 site in 1 country1,000 target enrollmentStarted: April 30, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
1,000
Locations
1
Primary Endpoint
Analysis of Respiratory Distress and Antithrombolytic Therapy in Patients with covid19

Study Overview

Brief 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

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Outcomes

Primary Outcomes

Analysis of Respiratory Distress and Antithrombolytic Therapy in Patients with covid19

Time Frame: 1 month

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital, Strasbourg, France
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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