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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04405869
Other study ID # 7779
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 29, 2020
Est. completion date April 2021

Study information

Verified date May 2020
Source University Hospital, Strasbourg, France
Contact Charles TACQUARD, MD
Phone 33 3 69 55 16 08
Email charlesambroise.tacquard@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main objective of this study is to describe the incidence of thromboembolic events in a population of patients hospitalized in intensive care units in France for severe COVID-19. The secondary objective of this study is to describe the evolution of hemostasis parameters during the first two weeks of intensive care hospitalization and to evaluate the influence of different anticoagulation regimens on these parameters and on the incidence of thromboembolic events


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date April 2021
Est. primary completion date April 2021
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Confirmed infection with the Sars-CoV-2 virus (RT-PCR)

- Hospitalization in Intensive Care Unit

- Age over 18 years Old

Exclusion Criteria:

- Refusal of the patient to participate in data collection

Study Design


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 incidence of thromboembolic events in patients with Sars-CoV-2 1 month
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