Skip to content

Effect of tranexamic acid on the incidence of early graft dysfunction during orthotopic liver transplantation: a randomized controlled trial

Effect of tranexamic acid on the incidence of early graft dysfunction during orthotopic liver transplantation: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300079022
Enrollment
Unknown
Registered
2023-12-23
Start date
2023-12-25
Completion date
Unknown
Last updated
2024-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

liver transplantation

Interventions

tranexamic acid group :After anesthesia induction, in the tranexamic acid group, tranexamic acid is infused at a rate of 10 mg/kg/h until opening of the portal vein
control group:In the control group, the normal saline is infused at the same way.

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Adult patients =18 years old (2) Patients undergoing orthotopic liver transplantation under general anesthesia

Exclusion criteria

Exclusion criteria: (1) Acute arterial or venous embolism occurred within one month before surgery; (2) Patients with history of thrombophilia and Budd-Chiari Syndrome patients; (3) Patients with acute liver failure; (4) Patients undergoing retransplantation within one month; (5) Patients with renal disfunction requiring dialysis before operation; (6) Patients with epilepsy history; (7) Patients with a history of subarachnoid hemorrhage within one month before surgery or previous brain surgery; (8)Patients with allergy history to tranexamic acid, or have contraindications to tranexamic acid; (9) Refused to sign a consent form

Design outcomes

Primary

MeasureTime frame
the incidence of early allograft dysfunction;

Secondary

MeasureTime frame
Thromboembolism incidence rate;Intraoperative blood loss and autologous blood recovery and infusion volume;Red blood cell infusion volume;The incidence of acute renal function injury;coagulation;Hospitalization duration and expenses;Other adverse events after surgery;

Countries

China

Contacts

Public ContactYajie Zhang

Department of Anesthesiology, West China Hospital, Sichuan University

yajie_zhang2023@163.com+86 135 4808 3692

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 8, 2026