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Clinical Trials/NCT04278066
NCT04278066CompletedNot Applicable

Hyper-Cardia Study : Hyperoxia and Pulmonary Complications After Cardiac Surgery

University Hospital, Strasbourg, France1 site in 1 country300 target enrollmentStarted: February 5, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
300
Locations
1
Primary Endpoint
Retrospective study of the average of per and postoperative PaO2 in cardiac surgery

Study Overview

Brief Summary

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

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

  • 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

Outcomes

Primary Outcomes

Retrospective study of the average of per and postoperative PaO2 in cardiac surgery

Time Frame: iles analyzed retrospectily from January 1st, 2015 to December 31, 2019 will be examined

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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