Overview

Topical Effect of Tranexamic Acid in Postoperative Bleeding and Blood Products Transfusion After Cardiac Surgery

Status:
Completed
Trial end date:
2023-01-06
Target enrollment:
0
Participant gender:
All
Summary
This is a single-center, double-blind, randomized controlled trial (RCT) comparing two groups of application of topical dose of tranexamic acid (TxA) versus placebo in patients undergoing coronary artery bypass graft (CABG), off pump coronary bypass graft cardiac surgery (OPCAB), and adult heart valve surgery. The primary outcomes of this study comprised of two parameters; post operative bleeding and blood product transfusion. The primary outcomes were assessed during the operation, until 48-hour post operative.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Indonesia University
Treatments:
Tranexamic Acid
Criteria
Inclusion Criteria:

- Patients ages > 18 years old

- Patients who are scheduled electively for cardiac surgery in National Heart Center
Harapan Kita, Jakarta, Indonesia

- Patients with heart valve disease indicated for aortic or mitral repair/replace

- Patients with coronary artery disease indicated for CABG or OPCAB surgery

- Aortic and/ mitral valve surgery concomitant with tricuspid repair

- Patients who are agreed to participate in this study

Exclusion Criteria:

- Not willing to become research subjects

- Allergy to tranexamic acid

- Undergoing minimally invasive surgery

- Undergoing double valve (aorta & mitral) procedure and double procedure (CABG+valve,
valve+maze)

- Emergency surgery

- History of bleeding disorder or coagulopathy

- History of thromboembolic or hemorrhagic disease

- Active Infective endocarditis

- History of previous cardiac surgery

- Estimated glomerular filtration rate <30 mL/min or on dialysis

- Receiving oral therapy with clopidogrel, aspirin, dabigatran, or rivaroxaban in the
last five days

- Receiving chronic warfarin therapy who have not stopped their medication and have an
international normalized ratio (INR) >1.5 before surgery

- Pre-operative thrombocytopenia (<50,000 platelets per µL)

- Pregnancy or breast feeding

- Refusal of blood products

- Pericarditis