Skip to content

A Clinical Study for Portal Vein Embolization and Liver Venous Deprivation

A Clinical Study for Portal Vein Embolization and Liver Venous Deprivation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900028694
Enrollment
Unknown
Registered
2019-12-31
Start date
2020-01-01
Completion date
Unknown
Last updated
2020-01-06

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

Conditions

Primary hepatocellular carcinoma

Interventions

PVE group :PVE treatment
LVD group :LVD treatment

Sponsors

The First Affiliated Hospital of USTC
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-75 years old, male and female; (2) Hepatocellular carcinoma (HCC) diagnosed by histopathology, immunohistochemistry or imaging examination, which is too large to be resected by one-stage operation; (3) There was no distant metastasis; (4) FLR was less than 20% in patients with normal liver function, less than 30% in patients with fatty liver and chemotherapy, and less than 40% in patients with compensatory cirrhosis; (5) Except for liver-related functions, other main organs function normally; (6) Subjects volunteered to join the study, signed informed consent, good compliance, with follow-up; (7) Researchers believe that patients can benefit.

Exclusion criteria

Exclusion criteria: (1) The subjects withdrew their consent; (2) Adverse reactions; (3) No treatment due to progress; (4) Death of patients; (5) Loss of follow-up; (6) Other.

Design outcomes

Primary

MeasureTime frame
Increased liver volume;

Countries

China

Contacts

Public ContactLiu Lianxin

The First Affiliated Hospital of USTC

liulx@ustc.edu.cn+86 18096656677

Outcome results

None listed

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