COVID-19 Respiratory Distress and Antithrombotic Drugs in Subject's Habits
CRASH
1 other identifier
observational
1,000
1 country
1
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 30, 2020
CompletedFirst Submitted
Initial submission to the registry
May 27, 2020
CompletedFirst Posted
Study publicly available on registry
June 2, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2021
CompletedJanuary 11, 2021
May 1, 2020
1.1 years
May 27, 2020
January 8, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Analysis of Respiratory Distress and Antithrombolytic Therapy in Patients with covid19
1 month
Eligibility Criteria
Adult Partients hospitalised in HUS or GHRMSA for COVID-19 with diagnosis COVID-19 confirmed by smear or evoked by CT scan or chest X-ray without a differential diagnosis retained in the medical record
You may qualify if:
- 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
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Service Médecine Intensive et Réanimation
Strasbourg, 67091, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 27, 2020
First Posted
June 2, 2020
Study Start
April 30, 2020
Primary Completion
June 1, 2021
Study Completion
June 1, 2021
Last Updated
January 11, 2021
Record last verified: 2020-05