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
About this trial
This is an interventional prevention trial for Bleeding focused on measuring Tranexamic Acid, Cardiac surgery
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 )
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
NCT ID
NCT03376061
First Posted
November 17, 2017
Last Updated
January 26, 2021
Sponsor
Population Health Research Institute
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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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.
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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.
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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.
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PubMed Identifier
16400465
Citation
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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.
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PubMed Identifier
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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.
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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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Decreasing Postoperative Blood Loss by Topical vs. Intravenous Tranexamic Acid in Open Cardiac Surgery
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