Skip to content

A Study of the Correlation Between Portal Vein Thrombosis and Prognosis of Liver Transplantation

A Study of the Correlation Between Portal Vein Thrombosis and Prognosis of Liver Transplantation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06513780
Enrollment
700
Registered
2024-07-22
Start date
2016-01-01
Completion date
2025-12-31
Last updated
2025-09-18

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

Conditions

Portal Vein Thrombosis

Brief summary

The goal of this observational study is to investigate the correlation between portal vein thrombosis (PVT) and the prognosis of liver transplantation. The main questions it aims to address are: What is the prevalence of PVT? What are the risk factors associated with PVT? What is the prognostic impact of preoperative PVT on liver transplantation? Participants are divided into two groups: the PVT group and the non-PVT group. The investigators will comparatively analyze the data of both groups, estimate the prevalence and risk factors of PVT, construct a predictive model for PVT that is applicable in clinical settings, and clarify the prognostic effects of PVT.

Detailed description

The investigators aim to investigate the prevalence and risk factors of PVT, to develop a novel grading or rating system for PVT, and to explore the prognostic impact of preoperative PVT in liver transplantation. The investigators will: Recruit patients according to the inclusion/exclusion criteria and obtain signed informed consents. They will collect demographic and laboratory characteristics and classify patients into the PVT group and the non-PVT group based on preoperative ultrasound and/or computed tomography. Collect patients' perioperative medical imaging, surgical procedures, pathology reports, postoperative treatments, follow-up data, and clinical endpoints. Comparatively analyze the data of the PVT and non-PVT groups, estimate the prevalence and risk factors of PVT, construct a predictive model for PVT that is applicable in clinical settings, clarify the prognostic effects of PVT, and propose a grading/rating system for PVT.

Interventions

OTHERObservation

No intervention were made.

Sponsors

Ru-zhou Cai
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

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

Inclusion criteria

1. Liver transplantation recipients 2. Aged 18 years or older.

Exclusion criteria

1. Retransplantation 2. Multi-organ transplantation 3. Portal vein tumor thrombus

Design outcomes

Primary

MeasureTime frameDescription
Death10 yearsRate of death from various causes after liver transplant
Postoperative portal vein thrombosis10 yearsNumber of participants with portal vein thrombosis after liver transplant
Postoperative portal vein stenosis10 yearsNumber of participants with portal vein stenosis after liver transplant

Secondary

MeasureTime frameDescription
Postoperative complications1 yearRate of re-surgery, interventional operation, endoscopy, dialysis, etc.

Countries

China

Contacts

Primary ContactRu-zhou Cai, M.D.
18722563616@126.com18722563616

Outcome results

None listed

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