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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04278066
Other study ID # 7655
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 5, 2020
Est. completion date September 5, 2020

Study information

Verified date February 2020
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main objective is to demonstrate that hyperoxia in cardiac surgery increase the occurrence of post-operative pulmonary complications


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date September 5, 2020
Est. primary completion date September 5, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patient (=18 years old) - Patient operated heart surgery with extra-corporal life support - Hospitalization in Cardiology intensive and critical care unit - Patient operated in HUS between 01/01/2015 and 31/12/2019 - Subject consent, after information, to the reuse of its data for the purposes of this study Exclusion Criteria: - Non-consent patient - Hypoxemic patient - Emergency surgery - Patient with post-operative cardiac assist device - Patient with guardianship

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service d'Anesthésiologie - NHC 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 Retrospective study of the average of per and postoperative PaO2 in cardiac surgery iles analyzed retrospectily from January 1st, 2015 to December 31, 2019 will be examined
See also
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