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Decreasing Postoperative Blood Loss by Topical vs. Intravenous Tranexamic Acid in Open Cardiac Surgery (DEPOSITION)

Primary Purpose

Bleeding, Surgical Blood Loss

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Tranexamic Acid
Sponsored by
Population Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Bleeding focused on measuring Tranexamic Acid, Cardiac surgery

Eligibility Criteria

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

Inclusion Criteria:

  • Male or female >= 18 years old
  • Undergoing cardiac surgical procedure with the use of cardiopulmonary bypass and median sternotomy
  • Provide written informed consent

Exclusion Criteria:

  • Poor (English) language comprehension
  • Minimally invasive valve surgery
  • Off-pump procedures
  • Emergency operations
  • Known history of increased bleeding disorder
  • Thromboembolic disease
  • Allergy to tranexamic acid
  • Severe renal impairment (eGFR <30 mL/min/1.73m2 )

Sites / Locations

  • Hamilton General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

TA Topical

TA Intravenous

Arm Description

1 syringe of 50ml of topical Tranexamic Acid (5g) or placebo. The topical will be poured into the pericardial mediastinal cavities in 2 equal doses, 25ml when the pt comes off-pump and the other 25ml before sternotomy is closed.

2 syringes of 50ml (5mg) Tranexamic Acid for intravenous injection or placebo.

Outcomes

Primary Outcome Measures

Median Volume of Mediastinal Fluid Collected From Participants
Cumulative volume (mL) of fluid collected from mediastinal drainage tubes 24 hours after the surgical procedure

Secondary Outcome Measures

Number of Participants With Seizures
Patients experiencing a post-operative seizure
Number of Participants With Mortality
The occurrence of death due to any cause
Number of Participants With RBC Transfusion
Patients requiring a red blood cell transfusion
Number of Participants With Re-operation for Bleeding or Tamponade
Occurrence of re-operation for the purpose of bleeding or cardiac tamponade
Median Number of Hours Participants Spent in ICU
Number of hours participants spent in the intensive care unit (ICU)
Mean Concentration of TxA in Plasma Collected From Participants
Plasma TxA concentrations measured from blood samples taken upon arrival in the ICU

Full Information

First Posted
November 17, 2017
Last Updated
January 26, 2021
Sponsor
Population Health Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT03376061
Brief Title
Decreasing Postoperative Blood Loss by Topical vs. Intravenous Tranexamic Acid in Open Cardiac Surgery
Acronym
DEPOSITION
Official Title
DEPOSITION: Pilot Study Decreasing Postoperative Blood Loss by Topical vs. Intravenous Tranexamic Acid in Open Cardiac Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
December 21, 2017 (Actual)
Primary Completion Date
September 4, 2018 (Actual)
Study Completion Date
September 4, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Population Health Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim is to conduct a double-blinded single-centre randomized controlled clinical trial of application of topical dose of tranexamic acid (TA) versus the usual intravenous TA in patients undergoing cardiac surgery at the Hamilton General Hospital. This pilot study will assess the feasibility to perform a large randomized international trial exploring this objective.
Detailed Description
Postoperative bleeding related to open cardiac surgery increases the rates of complications and mortality. It results from the blood thinners that are needed for use. Intravenous tranexamic acid (TA) has become a mainstay in cardiac surgical procedures for decreasing bleeding and minimizing transfusion requirements. Although intravenous TA is usually well tolerated, there is a well-known risk (1 to 4%) of postoperative seizures. This is due to the similarity between TA and the brain tissues. The aim is to eliminate the risk of seizures but to maintain the protection against bleeding. When TA is used directly on the tissues (topically) for other type of surgeries (joints), TA is effective to reduce blood loss and transfusions. The aim is to prove that direct application of TA on the heart can eliminate postoperative seizures and reduce the amount of blood transfusions in patients who have cardiac surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bleeding, Surgical Blood Loss
Keywords
Tranexamic Acid, Cardiac surgery

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Tranexamic Acid intravenous + Placebo topical versus Placebo intravenous + Tranexamic Acid topical
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The pharmacy will prepare 1 syringe of 50 ml of topical TA (5 g) or placebo. They will also prepare for the same patient 2 syringes of 50 ml (5 g) for intravenous (i.v.) injection or placebo. TA is similar in all aspects to normal saline. Blinding of both teams will be easy. The syringes will be prepared and randomized in pharmacy before the surgery.
Allocation
Randomized
Enrollment
97 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TA Topical
Arm Type
Active Comparator
Arm Description
1 syringe of 50ml of topical Tranexamic Acid (5g) or placebo. The topical will be poured into the pericardial mediastinal cavities in 2 equal doses, 25ml when the pt comes off-pump and the other 25ml before sternotomy is closed.
Arm Title
TA Intravenous
Arm Type
Active Comparator
Arm Description
2 syringes of 50ml (5mg) Tranexamic Acid for intravenous injection or placebo.
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid
Other Intervention Name(s)
Cyklokapron
Intervention Description
Tranexamic Acid is a medication used to treat or prevent excessive blood loss from major trauma, post partum, surgery, tooth removal, nose bleeds, and heavy menstruation.
Primary Outcome Measure Information:
Title
Median Volume of Mediastinal Fluid Collected From Participants
Description
Cumulative volume (mL) of fluid collected from mediastinal drainage tubes 24 hours after the surgical procedure
Time Frame
Fluid collected in the first 24 hours after the surgical procedure
Secondary Outcome Measure Information:
Title
Number of Participants With Seizures
Description
Patients experiencing a post-operative seizure
Time Frame
Patients will be followed post-operatively until hospital discharge
Title
Number of Participants With Mortality
Description
The occurrence of death due to any cause
Time Frame
Patients will be followed post-operatively until hospital discharge
Title
Number of Participants With RBC Transfusion
Description
Patients requiring a red blood cell transfusion
Time Frame
Intra-operative and post-operative RBC transfusions
Title
Number of Participants With Re-operation for Bleeding or Tamponade
Description
Occurrence of re-operation for the purpose of bleeding or cardiac tamponade
Time Frame
Patients will be followed post-operatively until hospital discharge
Title
Median Number of Hours Participants Spent in ICU
Description
Number of hours participants spent in the intensive care unit (ICU)
Time Frame
Number of hours spent in ICU from arrival to exit (collected at the Post-Operative Visit).
Title
Mean Concentration of TxA in Plasma Collected From Participants
Description
Plasma TxA concentrations measured from blood samples taken upon arrival in the ICU
Time Frame
on arrival in ICU within 3 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female >= 18 years old Undergoing cardiac surgical procedure with the use of cardiopulmonary bypass and median sternotomy Provide written informed consent Exclusion Criteria: Poor (English) language comprehension Minimally invasive valve surgery Off-pump procedures Emergency operations Known history of increased bleeding disorder Thromboembolic disease Allergy to tranexamic acid Severe renal impairment (eGFR <30 mL/min/1.73m2 )
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andre Lamy, MD MHSc
Organizational Affiliation
Population Health Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamilton General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
3766524
Citation
Kucuk O, Kwaan HC, Frederickson J, Wade L, Green D. Increased fibrinolytic activity in patients undergoing cardiopulmonary bypass operation. Am J Hematol. 1986 Nov;23(3):223-9. doi: 10.1002/ajh.2830230306.
Results Reference
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PubMed Identifier
6448643
Citation
Harker LA, Malpass TW, Branson HE, Hessel EA 2nd, Slichter SJ. Mechanism of abnormal bleeding in patients undergoing cardiopulmonary bypass: acquired transient platelet dysfunction associated with selective alpha-granule release. Blood. 1980 Nov;56(5):824-34. No abstract available.
Results Reference
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PubMed Identifier
8283896
Citation
Despotis GJ, Santoro SA, Spitznagel E, Kater KM, Cox JL, Barnes P, Lappas DG. Prospective evaluation and clinical utility of on-site monitoring of coagulation in patients undergoing cardiac operation. J Thorac Cardiovasc Surg. 1994 Jan;107(1):271-9.
Results Reference
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PubMed Identifier
7508070
Citation
Lemmer JH Jr, Stanford W, Bonney SL, Breen JF, Chomka EV, Eldredge WJ, Holt WW, Karp RB, Laub GW, Lipton MJ, et al. Aprotinin for coronary bypass operations: efficacy, safety, and influence on early saphenous vein graft patency. A multicenter, randomized, double-blind, placebo-controlled study. J Thorac Cardiovasc Surg. 1994 Feb;107(2):543-51; discussion 551-3.
Results Reference
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PubMed Identifier
16400465
Citation
Santos AT, Kalil RA, Bauemann C, Pereira JB, Nesralla IA. A randomized, double-blind, and placebo-controlled study with tranexamic acid of bleeding and fibrinolytic activity after primary coronary artery bypass grafting. Braz J Med Biol Res. 2006 Jan;39(1):63-9. doi: 10.1590/s0100-879x2006000100007. Epub 2005 Dec 15.
Results Reference
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PubMed Identifier
12651635
Citation
Pleym H, Stenseth R, Wahba A, Bjella L, Karevold A, Dale O. Single-dose tranexamic acid reduces postoperative bleeding after coronary surgery in patients treated with aspirin until surgery. Anesth Analg. 2003 Apr;96(4):923-928. doi: 10.1213/01.ANE.0000054001.37346.03.
Results Reference
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PubMed Identifier
27774838
Citation
Myles PS, Smith JA, Forbes A, Silbert B, Jayarajah M, Painter T, Cooper DJ, Marasco S, McNeil J, Bussieres JS, McGuinness S, Byrne K, Chan MT, Landoni G, Wallace S; ATACAS Investigators of the ANZCA Clinical Trials Network. Tranexamic Acid in Patients Undergoing Coronary-Artery Surgery. N Engl J Med. 2017 Jan 12;376(2):136-148. doi: 10.1056/NEJMoa1606424. Epub 2016 Oct 23. Erratum In: N Engl J Med. 2018 Feb 22;378(8):782.
Results Reference
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PubMed Identifier
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Citation
Martin K, Wiesner G, Breuer T, Lange R, Tassani P. The risks of aprotinin and tranexamic acid in cardiac surgery: a one-year follow-up of 1188 consecutive patients. Anesth Analg. 2008 Dec;107(6):1783-90. doi: 10.1213/ane.0b013e318184bc20.
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Kalavrouziotis D, Voisine P, Mohammadi S, Dionne S, Dagenais F. High-dose tranexamic acid is an independent predictor of early seizure after cardiopulmonary bypass. Ann Thorac Surg. 2012 Jan;93(1):148-54. doi: 10.1016/j.athoracsur.2011.07.085. Epub 2011 Nov 4.
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Decreasing Postoperative Blood Loss by Topical vs. Intravenous Tranexamic Acid in Open Cardiac Surgery

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