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
| Type | Name | Description |
|---|---|---|
| OTHER | standard of care | retrospective 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.