Postoperative Morbidity and Mortality After Cardiac Surgery
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris
About this trial
The local database results from a joint initiative of anesthesic, cardiology and cardiac surgery departements.Its purpose is to record in an exhaustive fashion all the interventions of cardiac surgery performed under extracorporeal circulation in adults at Bichat hospital.This database includes the preoperative characteristics of the patients, the type of surgery, the post-operative complications and the in-hospital mortality. The purpose of this observational study is to evaluate in-hospital morbidity and mortality for all types of cardiac surgery interventions and to analyze it according to the characteristics of the patients and the type of intervention.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
18 years and older and has legal capacity - cardiac surgery under extra corporeal circulation
non objection to record medical information during hospitalization
Disqualifiers
None
Trial population
all patients , 18 years old and older, with a cardiac surgery under extra corporeal circulation in Bichat Hospital
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
All-cause mortality
All-cause mortality is assessed during in-hospital stay and 30 days after the date of surgery
Time frame
30 daysSecondary outcomes
1
Postoperative organ failure
Cardiac with inotropic or mechanical support, renal failure or need for dialysis, pulmonary (mechanical ventilation duration), neurologic or digestive complications
Time frame
30 days2
Bleeding complications
Total blood loss, transfusion requirements, surgical reexploration
Time frame
30 days3
Arrhythmias
Atrial fibrillation, ventricular tachycardia
Time frame
30 days4
Conductions disturbances
Need for pace maker implantation
Time frame
30 daysSponsors and contacts
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Source ClinicalTrials.gov