Skip to content

Donor and recipient selective criteria for adult split liver transplantation: a retrospective multicenter research

Donor and recipient selective criteria for adult split liver transplantation: a retrospective multicenter research

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110745
Enrollment
Unknown
Registered
2025-10-20
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Adult end-stage liver disease

Interventions

Group of split liver transplantation:None
Group of whole liver transplantation:None

Sponsors

The First Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Male or female adult liver transplant recipients (aged 18 to 70 years); (2) Undergoing liver transplantation and long-term follow-up in six transplant centers; (3) Conscious, without severe intellectual, mental or neurological disorders.

Exclusion criteria

Exclusion criteria: (1) Other factors that the researcher deems may affect the safety of the subjects or their compliance with the trial. (2) Subjects with brain diseases, mental developmental abnormalities, or inability to cooperate with the research. (3) Those with extremely poor compliance, dropping out by more than 30% or missing follow-up visits twice or more consecutively.

Design outcomes

Primary

MeasureTime frame
EAD rate;The incidence of perioperative (90-day) complications in liver transplant recipients;Perioperative survival rate (90 days);

Secondary

MeasureTime frame
Overall survival time and survival rate of the recipients;Survival time and survival rate of the graft;

Countries

China

Contacts

Public ContactTingbo Liang

The First Affiliated Hospital, Zhejiang University School of Medicine

liangtingbo@zju.edu.cn+86 571 8723 6601

Outcome results

None listed

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