Clinical Trials Directory

Trials / Completed

CompletedNCT04804345

AProtinin Versus Tranexamic Acid in Cardiac Surgery Patients With High-risk for Excessive Bleeding

Status
Completed
Phase
Study type
Observational
Enrollment
693 (actual)
Sponsor
University Hospital, Bordeaux · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In this before-after multicenter study the authors tested the hypothesis that the prophylactic use of aprotinin compared to tranexamic acid could reduce the proportion of patients presenting severe perioperative bleeding.

Detailed description

Perioperative bleeding remains a real challenge for physicians managing cardiac surgical patients. In patients at high risk for excessive bleeding the prophylactic use of antifibrinolytics may be useful. This study propose to compare the efficacity and innocuity of aprotinin and tranexamic acid to reduce the proportion of patient presenting severe peri-operative bleeding according the Universal Definition of Perioperative Bleeding (UDPB) classification.

Conditions

Interventions

TypeNameDescription
OTHERstandard of careretrospective study: standard of care

Timeline

Start date
2021-03-31
Primary completion
2021-08-31
Completion
2021-08-31
First posted
2021-03-18
Last updated
2022-03-03

Locations

7 sites across 1 country: France

Source: ClinicalTrials.gov record NCT04804345. Inclusion in this directory is not an endorsement.