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Comparison of Aprotinin and Tranexamic Acid in Routine Cardiac Surgery

Primary Purpose

Bleeding and Cardiac Surgery, Allogeneic Blood Transfusion, Aortic Valve Replacement

Status
Unknown status
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
aprotinin or tranexamic acid
Sponsored by
German Heart Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Bleeding and Cardiac Surgery focused on measuring cardiac surgery, blood transfusion, antifibrinolytics, aprotinin, tranexamic acid

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • German Heart Center Munich

Outcomes

Primary Outcome Measures

24 hours postoperative drainage blood loss
incidence of allogeneic blood transfusion

Secondary Outcome Measures

activation of fibrinolysis and hemostasis
impairment of renal function

Full Information

First Posted
November 6, 2006
Last Updated
November 6, 2006
Sponsor
German Heart Center
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1. Study Identification

Unique Protocol Identification Number
NCT00396760
Brief Title
Comparison of Aprotinin and Tranexamic Acid in Routine Cardiac Surgery
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
November 2006
Overall Recruitment Status
Unknown status
Study Start Date
January 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
German Heart Center

4. Oversight

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bleeding and Cardiac Surgery, Allogeneic Blood Transfusion, Aortic Valve Replacement, Coronary Artery Bypass Graft Surgery
Keywords
cardiac surgery, blood transfusion, antifibrinolytics, aprotinin, tranexamic acid

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
220 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
aprotinin or tranexamic acid
Primary Outcome Measure Information:
Title
24 hours postoperative drainage blood loss
Title
incidence of allogeneic blood transfusion
Secondary Outcome Measure Information:
Title
activation of fibrinolysis and hemostasis
Title
impairment of renal function

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wulf Dietrich, MD, PhD
Organizational Affiliation
Department of Anesthesiology, German Heart Center Munich
Official's Role
Principal Investigator
Facility Information:
Facility Name
German Heart Center Munich
City
Munich
ZIP/Postal Code
80636
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
15591329
Citation
Diprose P, Herbertson MJ, O'Shaughnessy D, Deakin CD, Gill RS. Reducing allogeneic transfusion in cardiac surgery: a randomized double-blind placebo-controlled trial of antifibrinolytic therapies used in addition to intra-operative cell salvage. Br J Anaesth. 2005 Mar;94(3):271-8. doi: 10.1093/bja/aei044. Epub 2004 Dec 10.
Results Reference
background
PubMed Identifier
11279735
Citation
Henry DA, Moxey AJ, Carless PA, O'Connell D, McClelland B, Henderson KM, Sly K, Laupacis A, Fergusson D. Anti-fibrinolytic use for minimising perioperative allogeneic blood transfusion. Cochrane Database Syst Rev. 2001;(1):CD001886. doi: 10.1002/14651858.CD001886.
Results Reference
background
PubMed Identifier
17056936
Citation
Royston D, Levy JH, Fitch J, Dietrich W, Body SC, Murkin JM, Spiess BD, Nadel A. Full-dose aprotinin use in coronary artery bypass graft surgery: an analysis of perioperative pharmacotherapy and patient outcomes. Anesth Analg. 2006 Nov;103(5):1082-8. doi: 10.1213/01.ane.0000238447.74029.f5.
Results Reference
background
PubMed Identifier
17056935
Citation
Dietrich W, Busley R, Kriner M. High-dose aprotinin in cardiac surgery: is high-dose high enough? An analysis of 8281 cardiac surgical patients treated with aprotinin. Anesth Analg. 2006 Nov;103(5):1074-81. doi: 10.1213/01.ane.0000238446.30034.c8.
Results Reference
background
PubMed Identifier
21127274
Citation
Lison S, Dietrich W, Braun S, Boehm J, Schuster T, Englhard A, Perchuc A, Spannagl M, Busley R. Enhanced thrombin generation after cardiopulmonary bypass surgery. Anesth Analg. 2011 Jan;112(1):37-45. doi: 10.1213/ANE.0b013e3181fc6df0. Epub 2010 Dec 2.
Results Reference
derived
PubMed Identifier
18931201
Citation
Dietrich W, Spannagl M, Boehm J, Hauner K, Braun S, Schuster T, Busley R. Tranexamic acid and aprotinin in primary cardiac operations: an analysis of 220 cardiac surgical patients treated with tranexamic acid or aprotinin. Anesth Analg. 2008 Nov;107(5):1469-78. doi: 10.1213/ane.0b013e318182252b.
Results Reference
derived

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Comparison of Aprotinin and Tranexamic Acid in Routine Cardiac Surgery

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