Clinical Trials Directory

Trials / Unknown

UnknownNCT05457374

A Clinical Study of Portal Vein Embolization and Liver Venous Deprivation

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
Anhui Provincial Hospital · Other Government
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The main obstacle to achieving R0 resection in future liver remnant(FLR) deficient liver cancer is the inability to retain sufficient FLR to avoid postoperative liver failure. From the initial portal vein embolization(PVE), to the later ALPPS, this problem has been solved to some extent. However, both have their own shortcomings. The effect of liver hyperplasia after PVE is poor and the waiting time is long. The incidence of complication and mortality after ALPPS is always the focus of controversy. In recent years, LVD has emerged, combining PVE and HVE in the one operation. This topic will conduct a clinical controlled study of PVE and LVD.

Conditions

Interventions

TypeNameDescription
PROCEDUREPVEPortal vein embolization (PVE) mainly embolizes the portal vein of the resected liver lobe, causing the non-tumor lobe to proliferate, and after tumor lobectomy, the volume of the non-tumor lobe proliferates so that patients with hepatocellular carcinoma that could not be directly surgically resected are given the opportunity to be surgically resected
PROCEDURELVDCombining PVE and Hepatic Vein Embolization (HVE) in the same procedure

Timeline

Start date
2022-03-01
Primary completion
2024-03-01
Completion
2025-03-01
First posted
2022-07-14
Last updated
2022-07-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05457374. Inclusion in this directory is not an endorsement.