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The study of controlled low central venous pressure combined with different doses of tranexamic acid in hepatectomy

The study of controlled low central venous pressure combined with different doses of tranexamic acid in hepatectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076300
Enrollment
Unknown
Registered
2023-09-29
Start date
2023-10-08
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

hepatectomy

Interventions

Control group:Administer physiological saline as a placebo, with a loading capacity of 0.5 hours before surgery. Intravenous infusion of 100 mL of physiological saline is maintained at a volume of 1 m
TXA I group:Tranexamic Acid, the loading dose of tranexamic acid was 10 mg/kg intravenous infusion 0.5h before operation, and the maintenance dose was 1 mg/(kg·h) intravenous pump until the end of ope
TXA II group:Tranexamic Acid, the loading dose of tranexamic acid was 1g intravenous infusion 0.5h before operation, and the maintenance dose was 10 mg/(kg·h) intravenous pump until the end of operati

Sponsors

The Second Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients of both sexes, aged 18-70 years, undergoing first elective laparoscopic hepatectomy; 2. ASA I-II; 3. Child-Pugh A/B; 4. No accompanying other major surgical procedures, such as intestinal, biliary and pancreatic resection.

Exclusion criteria

Exclusion criteria: 1. Obese patients (BMI > 32 kg/m²); 2. Contraindications to the use of tranexamic acid; 3. Patients with disease of heart head blood-vessel II level and above (hypertension, arrhythmia, cardiomyopathy, myocardial infarction, cerebral infarction); 4. Pregnant or lactating women; 5. Any unstable condition that may endanger the safety and compliance of patients.

Design outcomes

Primary

MeasureTime frame
activated partial thromboplastin time, APTT;prothrombin time, PT;fibrinogen, FIB;fibrinogen degradation products, FDPS;Blood loss;the rate of transfusion;hospitalization expenses;

Secondary

MeasureTime frame
thrombin time, TT;D-dimer;hospital stays;

Countries

China

Contacts

Public ContactSi Yongyu

The Second Affiliated Hospital of Kunming Medical University

15559672131@163.com+86 158 1212 8771

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026