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Effect of Terlipressin on the Incidence of Early Postoperative Acute Kidney Injury in Liver Transplantation Patients

Effect of Intraoperative Terlipressin on the Incidence of Early Postoperative Acute Kidney Injury in Liver Transplantation Patients: a Randomized, Double-blind, Placebo-controlled Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06108362
Enrollment
104
Registered
2023-10-31
Start date
2023-08-18
Completion date
2024-06-30
Last updated
2023-10-31

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

Conditions

Acute Kidney Injury, Liver Transplant; Complications

Keywords

terlipressin, Liver Transplant

Brief summary

The goal of this clinical trial is to evaluate the effect of intraoperative terlipressin on the incidence of early postoperative acute kidney injury in deceased doner liver transplantation. Patients were randomly divided into experimental group and control group by numerical randomization table. The experimental group was injected with terlipressin perioperative and the control group was injected with placebo

Detailed description

acute kidney injury is a relatively common complication in patients with liver transplantation. Most centers have established prediction models for acute kidney injury after liver transplantation, but the incidence cannot be reduced through perioperative anesthesia management. As an vasopressin receptor agonist, terlipressin can increase blood pressure and improve kidney perfusion at the same time, and perioperative application may reduce the incidence of postoperative acute kidney injury

Interventions

DRUGTerlipressin

The medication is dispensed by the nursing staff before surgery and given to the anesthesiologist before the procedure begins

DRUGnormal saline

The medication is dispensed by the nursing staff before surgery and given to the anesthesiologist before the procedure begins

Sponsors

Beijing Tsinghua Chang Gung Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* 1\) Patients who plan to undergo liver transplantation in our hospital 2) Patients or family members sign informed consent

Exclusion criteria

* Patients \<18 years old;② Patients undergoing autologous liver transplantation or combined transplantation;③ Patients with lower extremity artery stenosis;(4) Patients with severe heart disease、lung disease、kidney disease;⑤ Patients with severe lung disease;⑥ Patients who used renal replacement therapy before surgery;⑦ the depth of one kidney from the body surface is greater than 4cm;⑧ Patients treated with terlipressin within 2 weeks before surgery⑨ Patients allergic to terlipressin.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of acute kidney injury after liver transplantationin 7 daysacute kidney injury diagnostic criteria (2012 edition)

Countries

China

Contacts

Primary ContactZiheng Qi, Doctor
469836626@qq.com15373598688

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026