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Anti-Xa Activity-Based Prophylaxis In Liver Transplantation Patients, a Prospective Multicenter Randomized Controlled Study

Anti-Xa Activity-Based Prophylaxis In Liver Transplantation Patients, a Prospective Multicenter Randomized Controlled Study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032441
Enrollment
Unknown
Registered
2020-04-28
Start date
2020-05-01
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Liver failure

Interventions

Control group:Intervention: The control group received a daily dose of normal saline (0.9% NaCl) within 24 hours following their surgery, with this regimen continuing until day 7 after transplantation
Anticoagulant group:Patients in the anticoagulant group received a daily dose of 40 mg of enoxaparin within 24 hours following their surgery and continued this regimen until day 7 after transplantatio

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) All orthotopic deceased-donor liver transplantation p/µLatients aged between 18 and 70 years. (2) Signed informed consent and able to comply with the requirements of the program; if the patient is unable to sign the informed consent form, his/her legal guardian or representative must sign it.

Exclusion criteria

Exclusion criteria: (1) Autotransplantation, living donor, split and pediatric liver transplantation. (2) Other ongoing anticoagulative therapy.

Design outcomes

Primary

MeasureTime frame
major bleeding events within the first 90 days post-LT;venous thrombosis events within the first 90 days post-LT;

Secondary

MeasureTime frame
Anti-Xa;PVT events within the first 90 days post-LT;DVT events within the first 90 days post-LT;

Countries

China

Contacts

Public ContactYong Zeng

West China Hospital, Sichuan University

zengyong@medmail.com.cn+86 189 8060 1472

Outcome results

None listed

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