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Comparison of Aprotinin and Tranexamic Acid in Routine Cardiac Surgery

The Influence of High-Dose Aprotinin and Tranexamic Acid on Bleeding Tendency and Allogeneic Blood Transfusion in Patients Undergoing Primary Aortic Valve Replacement or Coronary Artery Revascularization

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00396760
Enrollment
220
Registered
2006-11-07
Start date
2005-01-31
Completion date
2006-07-31
Last updated
2006-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allogeneic Blood Transfusion, Aortic Valve Replacement, Bleeding and Cardiac Surgery, Coronary Artery Bypass Graft Surgery

Keywords

cardiac surgery, blood transfusion, antifibrinolytics, aprotinin, tranexamic acid

Brief summary

The hypothesis of this study is that the antifibrinolytic drugs aprotinin and tranexamic acid equally influence bleeding tendency and transfusion requirement in patients undergoing first time cardiac procedures with a low risk of increased postoperative bleeding.Only patients undergoing first time CABG or first time aortic valve replacement are included in this study.

Detailed description

Excessive bleeding during and after cardiac surgery is a serious complication. It exposes patients to the risk of allogeneic blood transfusion or other blood products and the risk of mediastinal re-exploration.Antifibrinolytic drugs like aprotinin and tranexamic acid are proven to reduce bleeding tendency and transfusion requirement in cardiac surgery. The efficacy of these drugs is proven, especially for the unspecific proteinase inhibitor aprotinin, however, there are concerns about the safety and the high costs of this drug. There are only limited head-to-head comparisons of these two drugs. In this double-blind, prospective, controlled study the efficacy of aprotinin and tranexamic acid is compared. Primary outcome is the 24 hours postoperative drainage blood loss and the percentage of patients requiring allogeneic blood transfusion during the hospital stay. Subgroups of patients undergoing CABG surgery or aortic valve replacement are predefined for combined and separate data analysis.The power of the study is calculated for this subgroup-analysis. Secondary outcome measurements are molecular marker of activation of hemostasis up to the 5th postoperative day.

Interventions

DRUGaprotinin or tranexamic acid

Sponsors

German Heart Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* informed consent * Patients undergoing primary CABG or Aortic valve replacement surgery

Exclusion criteria

* Previous sternotomy * OPCAB surgery * urgent/emergency operation * Coumadin treatment * previous aprotinin exposure * preoperative renal impairment (Creatinine \> 2 mg/dL) * patients refusing blood transfusions * no informed consent

Design outcomes

Primary

MeasureTime frame
24 hours postoperative drainage blood loss
incidence of allogeneic blood transfusion

Secondary

MeasureTime frame
activation of fibrinolysis and hemostasis
impairment of renal function

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026