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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04362345
Other study ID # 7773
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 9, 2020
Est. completion date January 9, 2021

Study information

Verified date April 2020
Source University Hospital, Strasbourg, France
Contact Yves HANSMANN, MD, PhD
Phone 33 3 69 55 09 78
Email Yves.hansmann@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the research is to improve patient management by rapidly identifying, based on the terrain and clinical and biological characteristics, those patients likely to present a severe form of ARDS at risk of leading to intensive care


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date January 9, 2021
Est. primary completion date January 9, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Major patient (=18 years of age) - Admitted in March 2020 for confirmed Covid-19 lung disease (nasopharyngeal smear or sputum with SARS-CoV-2 positive PCR). Exclusion Criteria: - Patient who has expressed opposition to participation in the study. - Mild forms of infection that do not require hospitalization, - Subject under safeguard of justice - Subject under guardianship or trusteeship

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service des Maladies Infectieuses et Tropicales 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 Identification of risk factors for severity (death or transfer to resuscitation) of Covid-19 infection Files analysed retrospectively from March 1st, 2020 to April 15, 2020 will be examined]
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