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Goal-directed vs. Empirical Tranexamic Acid Administrationin Cardiovascular Surgery

Primary Purpose

Heart Diseases, Vascular Diseases, Transfusion Related Complication

Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
TXA administration
Placebo administration
Sponsored by
Konkuk University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Heart Diseases

Eligibility Criteria

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

Inclusion Criteria: patients who will undergo elective cardiovascular surgery employing cardiopulmonary bypass patients who provide written informed consent Exclusion Criteria: pregnancy refusal of allogenic blood transfusion taking thrombin history of thromboembolic and familial hypercoagulability disease recent history of myocardial infarction or ischemic cerebral infarction (within 90 days) hypersensitive to TXA histroy of convulsion or epilepsy taking hemodialysis history of Heparin-induced thrombocytopenia

Sites / Locations

  • Asan Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Experimental

Experimental

Arm Label

Empirical 1: TXA and Placebo administration

Empirical 2: TXA administration

Goal-directed 1: Placebo administration

Goal-directed 2: TXA and Placebo administration

Arm Description

Tranexamic acid administration, regardless of the result of rotational thromboelastometry. Placebo administration, at LI60 < 85 % or A10< 40 mm in EXTEM of rotational thromboelastometry

Tranexamic acid administration, regardless of the result of rotational thromboelastometry. Placebo discard, at LI60 ≥ 85% or A10 ≥ 40 mm in EXTEM of rotational thromboelastometry

Placebo administration, regardless of the result of rotational thromboelastometry. Tranexamic acid administration at LI60 < 85 % or A10 < 40 mm in EXTEM of rotational thromboelastometry

Placebo administration, regardless of the result of rotational thromboelastometry. Tranexamic acid discard at LI60 ≥ 85% or A10 ≥ 40 mm in EXTEM of rotational thromboelastometry

Outcomes

Primary Outcome Measures

postoperative bleeding
bleeding amount though chest drainage tubes during the 1st postoperative 24 hour

Secondary Outcome Measures

postoperative transfusion amount
amounts of transfused red blood cells, plasma, platelet and cryoprecipitate
postoperative transfusion rate
incidents of red blood cells, plasma, platelet and cryoprecipitate transfusions
the lowest postoperative hemoglobin value
the nadir hemoglobin value during one postoperative days
incidence of reoperation
incidence of reoperation due to postoperative bleeding
amount of intraoperative cell salvage
amounts of infused salvaged blood
viscoelastic whole blood profile
values of intraoperative CT-EXTEM, CFT-EXTEM, A10-EXTEM, MCF-EXTEM, ML-EXTEM, CT-FIBTEM, CFT-FIBTEM, A10-FIBTEM, MCF-FIBTEM, ML-FIBTEM in rotational thromboelastometry
incidence of seizure
incidence of postoperative seizure till the hospital discharge
incidence of thromboembolic complications
incidence of postoperative myocardia infarction, stroke, pulmonary embolism, gut infarction till the hospital discharge
duration of mechanical ventilation
duration of postoperative ventilatory care
length of stays in the ICU and hospital
total cost
total expense paid at the discharge
incidence of taking renal replacement therapy

Full Information

First Posted
March 28, 2023
Last Updated
September 12, 2023
Sponsor
Konkuk University Medical Center
Collaborators
Korea Health Industry Development Institute, Helptrial, Asan Medical Center, Samsung Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05806346
Brief Title
Goal-directed vs. Empirical Tranexamic Acid Administrationin Cardiovascular Surgery
Official Title
Tranexamic Acid Administration Strategies in Cardiovascular Surgery: Goal-directed Tranexamic Acid Administration Based on Viscoelastic Test vs. Empirical Tranexamic Acid Administration
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2023 (Actual)
Primary Completion Date
August 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Konkuk University Medical Center
Collaborators
Korea Health Industry Development Institute, Helptrial, Asan Medical Center, Samsung Medical Center

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 present study is a multi-center randomized prospective placebo-controlled non-inferiority trial. The study's primary objective is to compare the amounts of postoperative bleeding using two different TXA administration strategies: empirical TXA administration vs. viscoelastic test-based goal-directed TXA administration in cardiovascular surgery. The secondary objectives include comparing the incidents of hyper-fibrinolysis, thromboembolic complications, and postoperative seizures. Researchers assumed that goal-directed tranexamic acid (TXA) administration using viscoelastic field tests would not be inferior to the empirical TXA administration strategy in reducing postoperative bleeding and hyper-fibrinolysis. It also would be beneficial in lowering TXA-induced thromboembolic complications and seizures.
Detailed Description
The present study is a multi-center randomized prospective placebo-controlled non-inferiority trial. This study's primary objective is to compare the amounts of postoperative bleeding during postoperative 24 hours through chest tube drainage using two different tranexamic acid (TXA) administration strategies: empirical TXA administration vs. viscoelastic test-based goal-directed TXA administration in cardiovascular surgery. The secondary objectives include determining the inter-group differences in hyper-fibrinolysis, thromboembolic complications, and postoperative seizures. Researchers hypothesized that goal-directed TXA administration using viscoelastic field tests would not be inferior to the empirical TXA administration strategy in reducing postoperative bleeding and hyper-fibrinolysis. Researchers also expect that goal-directed TXA administration would be beneficial in lowering TXA-induced thromboembolic complications and seizure risks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Diseases, Vascular Diseases, Transfusion Related Complication, Coagulation Disorder, Blood, Fibrinolysis; Hemorrhage

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized prospective double-blind placebo-controlled multicenter non-inferior
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
placebo-controlled
Allocation
Randomized
Enrollment
764 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Empirical 1: TXA and Placebo administration
Arm Type
Active Comparator
Arm Description
Tranexamic acid administration, regardless of the result of rotational thromboelastometry. Placebo administration, at LI60 < 85 % or A10< 40 mm in EXTEM of rotational thromboelastometry
Arm Title
Empirical 2: TXA administration
Arm Type
Active Comparator
Arm Description
Tranexamic acid administration, regardless of the result of rotational thromboelastometry. Placebo discard, at LI60 ≥ 85% or A10 ≥ 40 mm in EXTEM of rotational thromboelastometry
Arm Title
Goal-directed 1: Placebo administration
Arm Type
Experimental
Arm Description
Placebo administration, regardless of the result of rotational thromboelastometry. Tranexamic acid administration at LI60 < 85 % or A10 < 40 mm in EXTEM of rotational thromboelastometry
Arm Title
Goal-directed 2: TXA and Placebo administration
Arm Type
Experimental
Arm Description
Placebo administration, regardless of the result of rotational thromboelastometry. Tranexamic acid discard at LI60 ≥ 85% or A10 ≥ 40 mm in EXTEM of rotational thromboelastometry
Intervention Type
Drug
Intervention Name(s)
TXA administration
Other Intervention Name(s)
Tranexamic acid
Intervention Description
Tranexamic acid intravenous administration
Intervention Type
Drug
Intervention Name(s)
Placebo administration
Other Intervention Name(s)
Placebo (normal saline)
Intervention Description
Placebo (normal saline) intravenous administration
Primary Outcome Measure Information:
Title
postoperative bleeding
Description
bleeding amount though chest drainage tubes during the 1st postoperative 24 hour
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
postoperative transfusion amount
Description
amounts of transfused red blood cells, plasma, platelet and cryoprecipitate
Time Frame
24 hours
Title
postoperative transfusion rate
Description
incidents of red blood cells, plasma, platelet and cryoprecipitate transfusions
Time Frame
24 hours
Title
the lowest postoperative hemoglobin value
Description
the nadir hemoglobin value during one postoperative days
Time Frame
24 hours
Title
incidence of reoperation
Description
incidence of reoperation due to postoperative bleeding
Time Frame
1 week
Title
amount of intraoperative cell salvage
Description
amounts of infused salvaged blood
Time Frame
1 hour
Title
viscoelastic whole blood profile
Description
values of intraoperative CT-EXTEM, CFT-EXTEM, A10-EXTEM, MCF-EXTEM, ML-EXTEM, CT-FIBTEM, CFT-FIBTEM, A10-FIBTEM, MCF-FIBTEM, ML-FIBTEM in rotational thromboelastometry
Time Frame
1 hour
Title
incidence of seizure
Description
incidence of postoperative seizure till the hospital discharge
Time Frame
1 week
Title
incidence of thromboembolic complications
Description
incidence of postoperative myocardia infarction, stroke, pulmonary embolism, gut infarction till the hospital discharge
Time Frame
1 week
Title
duration of mechanical ventilation
Description
duration of postoperative ventilatory care
Time Frame
1 week
Title
length of stays in the ICU and hospital
Time Frame
1 week
Title
total cost
Description
total expense paid at the discharge
Time Frame
2 week
Title
incidence of taking renal replacement therapy
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients who will undergo elective cardiovascular surgery employing cardiopulmonary bypass patients who provide written informed consent Exclusion Criteria: pregnancy refusal of allogenic blood transfusion taking thrombin history of thromboembolic and familial hypercoagulability disease recent history of myocardial infarction or ischemic cerebral infarction (within 90 days) hypersensitive to TXA histroy of convulsion or epilepsy taking hemodialysis history of Heparin-induced thrombocytopenia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Soi Lee
Phone
+82 10 4418 9288
Email
soileekku@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tae-Yop Kim, MD, PhD
Organizational Affiliation
Konkuk University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Asan Medical Center
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jaesik Nam
Email
jaesik_nam@naver.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Goal-directed vs. Empirical Tranexamic Acid Administrationin Cardiovascular Surgery

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