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The Effect on Blood Loss of Topical and Intravenous Tranexamic Acid in Cardiac Surgery Patients

Primary Purpose

Blood Loss, Tranexamic Acid, Cardiac Surgery

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
2 gr tranexamic acid
Saline
Sponsored by
Amphia Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Blood Loss focused on measuring blood loss, tranexamix acid, cardiac surgery

Eligibility Criteria

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

Inclusion Criteria:

  • Gender; male/ female
  • Age: ≥ 18 year
  • Elective cardiac surgical patients

    • Coronary artery bypass graft (CABG) (conventional, E.CCO)
    • Aortic valve replacement (AVR) (conventional)
    • Mitral valve replacement (MVR)/ Mitral valve repairment (MPL) (conventional)
    • Tricuspid valve replacement (TVR) / Tricuspid valve repairment (TPL)
    • Bentall
    • Combined procedure (e.g. CABG/ AVR, MVR/AVR, AVR/Maze)

Exclusion Criteria:

  • MVR/MPL (minimal invasive, Port Access Surgery)
  • Maze (minimal invasive, via Thoracoscopy)
  • AVR (minimal invasive, via mini Sternotomy)
  • off-pump procedures
  • Emergency operations
  • Patient with increased or decreased blooding tendency (FV leiden, prot C, S deficiency, anti-thrombin deficiency, prothrombin mutation)

Sites / Locations

  • Amphia Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

No Intervention

Experimental

Arm Label

pericardial lavage with 200 ml normothermic saline solution

No pericardial lavage

2 gr tranexamic acid diluted in 200 ml normothermic saline

Arm Description

According to the anaesthetic protocol of the Amphia Hospital (Breda, the Netherlands), all patients scheduled for cardiac surgery receive intravenously 2 gr TA before sternal incision and 2 gr TA after cardiopulmonary bypass. This arm also receives pericardial lavage with 200 ml normothermic saline solution without tranexamic acid.

According to the anaesthetic protocol of the Amphia Hospital (Breda, the Netherlands), all patients scheduled for cardiac surgery receive intravenously 2 gr TA before sternal incision and 2 gr TA after cardiopulmonary bypass. In this arm the subjects receives as in standard care no pericardial lavage.

According to the anaesthetic protocol of the Amphia Hospital (Breda, the Netherlands), all patients scheduled for cardiac surgery receive intravenously 2 gr TA before sternal incision and 2 gr TA after cardiopulmonary bypass. This arm receives also pericardial lavage with 2 gr TA diluted in 200 ml normothermic saline solution (NaCl 0.9%).

Outcomes

Primary Outcome Measures

Postoperative Blood Loss
The primary study parameter is 12 hours postoperative blood loss and is assessed by postoperative chest tube production. Postoperative chest tube production 12 hours after surgical procedure

Secondary Outcome Measures

Number of Participants Requiring Surgical Re-exploration
the secondary objective of this study is to determine whether pericardial lavage with saline gives an improvement in haemostasis, compared with no pericardial lavage, resulting in a reduction of surgical re-explorations and post-operative 12-hour blood loss. The choice for a surgical re-exploration will be decided according to the ICU protocol.
Total Red Blood Cell Transfusions (Cumulative of Pre, Peri and Postoperative Period)
The amount of red blood cell transfusions the patient receive pre, peri and postoperatively during their stay in the hospital.

Full Information

First Posted
June 25, 2013
Last Updated
May 1, 2015
Sponsor
Amphia Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01895101
Brief Title
The Effect on Blood Loss of Topical and Intravenous Tranexamic Acid in Cardiac Surgery Patients
Official Title
The Effect on Blood Loss of Topical and Intravenous Tranexamic Acid in Cardiac Surgery Patients: a Randomized Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
October 2013 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Amphia Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
It remains still unclear whether topical tranexamic acid has an added value besides the administration of intravenously tranexamic acid. We hypothesize that the addition of topical tranexamic acid, besides intravenous administration of tranexamic acid, results in a 25% reduction of post-operative blood loss after cardiac surgery. The aim of this study is to determine whether the application of topical tranexamic acid reduces the 12 hours postoperative blood loss by 25% in patient scheduled for cardiac surgery on cardiopulmonary bypass, whereby intravenous tranexamic acid is administrated. Just before sternal closure, 250 subjects receives pericardial lavage with 2 gr tranexamic acid in 200 ml normothermic saline solution (NaCl 0.9%), 250 subjects receives pericardial lavage with 200 ml normothermic saline solution without TA and 250 subjects (control group) receives no pericardial lavage. The main study parameter is 12 hours post-operative blood loss and is assessed by 12 hours post-operative chest tube production.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Blood Loss, Tranexamic Acid, Cardiac Surgery
Keywords
blood loss, tranexamix acid, cardiac surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
750 (Actual)

8. Arms, Groups, and Interventions

Arm Title
pericardial lavage with 200 ml normothermic saline solution
Arm Type
Placebo Comparator
Arm Description
According to the anaesthetic protocol of the Amphia Hospital (Breda, the Netherlands), all patients scheduled for cardiac surgery receive intravenously 2 gr TA before sternal incision and 2 gr TA after cardiopulmonary bypass. This arm also receives pericardial lavage with 200 ml normothermic saline solution without tranexamic acid.
Arm Title
No pericardial lavage
Arm Type
No Intervention
Arm Description
According to the anaesthetic protocol of the Amphia Hospital (Breda, the Netherlands), all patients scheduled for cardiac surgery receive intravenously 2 gr TA before sternal incision and 2 gr TA after cardiopulmonary bypass. In this arm the subjects receives as in standard care no pericardial lavage.
Arm Title
2 gr tranexamic acid diluted in 200 ml normothermic saline
Arm Type
Experimental
Arm Description
According to the anaesthetic protocol of the Amphia Hospital (Breda, the Netherlands), all patients scheduled for cardiac surgery receive intravenously 2 gr TA before sternal incision and 2 gr TA after cardiopulmonary bypass. This arm receives also pericardial lavage with 2 gr TA diluted in 200 ml normothermic saline solution (NaCl 0.9%).
Intervention Type
Drug
Intervention Name(s)
2 gr tranexamic acid
Intervention Description
This group receives pericardial lavage with 2 gr tranexamic diluted in 200 ml normothermic saline solution (NaCl 0.9%).
Intervention Type
Drug
Intervention Name(s)
Saline
Intervention Description
This group receives pericardial lavage with 200 ml normothermic saline solution without tranexamic acid
Primary Outcome Measure Information:
Title
Postoperative Blood Loss
Description
The primary study parameter is 12 hours postoperative blood loss and is assessed by postoperative chest tube production. Postoperative chest tube production 12 hours after surgical procedure
Time Frame
12 hours postoperative
Secondary Outcome Measure Information:
Title
Number of Participants Requiring Surgical Re-exploration
Description
the secondary objective of this study is to determine whether pericardial lavage with saline gives an improvement in haemostasis, compared with no pericardial lavage, resulting in a reduction of surgical re-explorations and post-operative 12-hour blood loss. The choice for a surgical re-exploration will be decided according to the ICU protocol.
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 2 days
Title
Total Red Blood Cell Transfusions (Cumulative of Pre, Peri and Postoperative Period)
Description
The amount of red blood cell transfusions the patient receive pre, peri and postoperatively during their stay in the hospital.
Time Frame
participants will be followed for the duration of ICU stay, an expected average of 2 days/ And participants will be followed for the duration of hospital stay, an expected average of 3 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Gender; male/ female Age: ≥ 18 year Elective cardiac surgical patients Coronary artery bypass graft (CABG) (conventional, E.CCO) Aortic valve replacement (AVR) (conventional) Mitral valve replacement (MVR)/ Mitral valve repairment (MPL) (conventional) Tricuspid valve replacement (TVR) / Tricuspid valve repairment (TPL) Bentall Combined procedure (e.g. CABG/ AVR, MVR/AVR, AVR/Maze) Exclusion Criteria: MVR/MPL (minimal invasive, Port Access Surgery) Maze (minimal invasive, via Thoracoscopy) AVR (minimal invasive, via mini Sternotomy) off-pump procedures Emergency operations Patient with increased or decreased blooding tendency (FV leiden, prot C, S deficiency, anti-thrombin deficiency, prothrombin mutation)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thierry Scohy
Organizational Affiliation
Amphia Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Amphia Hospital
City
Breda
ZIP/Postal Code
4800 RK
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
23063104
Citation
Mahaffey R, Wang L, Hamilton A, Phelan R, Arellano R. A retrospective analysis of blood loss with combined topical and intravenous tranexamic acid after coronary artery bypass graft surgery. J Cardiothorac Vasc Anesth. 2013 Feb;27(1):18-22. doi: 10.1053/j.jvca.2012.08.004. Epub 2012 Oct 10.
Results Reference
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PubMed Identifier
10694619
Citation
De Bonis M, Cavaliere F, Alessandrini F, Lapenna E, Santarelli F, Moscato U, Schiavello R, Possati GF. Topical use of tranexamic acid in coronary artery bypass operations: a double-blind, prospective, randomized, placebo-controlled study. J Thorac Cardiovasc Surg. 2000 Mar;119(3):575-80. doi: 10.1016/s0022-5223(00)70139-5.
Results Reference
background
PubMed Identifier
17218108
Citation
Baric D, Biocina B, Unic D, Sutlic Z, Rudez I, Vrca VB, Brkic K, Ivkovic M. Topical use of antifibrinolytic agents reduces postoperative bleeding: a double-blind, prospective, randomized study. Eur J Cardiothorac Surg. 2007 Mar;31(3):366-71; discussion 371. doi: 10.1016/j.ejcts.2006.12.003. Epub 2007 Jan 10.
Results Reference
background
PubMed Identifier
16438759
Citation
Abul-Azm A, Abdullah KM. Effect of topical tranexamic acid in open heart surgery. Eur J Anaesthesiol. 2006 May;23(5):380-4. doi: 10.1017/S0265021505001894. Epub 2006 Jan 27.
Results Reference
background
PubMed Identifier
21660523
Citation
Spegar J, Vanek T, Snircova J, Fajt R, Straka Z, Pazderkova P, Maly M. Local and systemic application of tranexamic acid in heart valve surgery: a prospective, randomized, double blind LOST study. J Thromb Thrombolysis. 2011 Oct;32(3):303-10. doi: 10.1007/s11239-011-0608-3.
Results Reference
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The Effect on Blood Loss of Topical and Intravenous Tranexamic Acid in Cardiac Surgery Patients

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