Skip to main content
Clinical Trials/NCT02145013
NCT02145013UnknownNot Applicable

Assessment and Impact of Portal Hypertension Before and During Liver Resection in Patients With Hepatocellular Carcinoma

Henri Mondor University Hospital1 site in 1 country200 target enrollmentStarted: November 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
Mortality

Study Overview

Brief Summary

According to the BCLC guidelines, surgical resection of hepatocellular carcinoma complicating cirrhosis is restricted to patients with preserved liver function, single nodule without vascular invasion and with hepatic venous gradient below 10 mmHg.

However, other guideline treatment, especially from eastern countries demonstrated that surgical resection is safe and feasible and provides better survival than the treatment recommended by the BCLC system for patients with similar stage.

The primary goal of this study is to assess the impact of HVPG on short and long-term outcomes in HCC patients who undergo liver resection.

Detailed Description

Patients with HCC and candidates for hepatectomy are classified into two groups according to the presence of portal hypertension. Short- and long-term outcomes will be compared.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Mortality

Time Frame: 90 day

In-hospital or 90-day mortality

Secondary Outcomes

  • morbidity(90 day)
  • Survival outcomes(1,3 and 5 years)

Investigators

Sponsor
Henri Mondor University Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Chetana LIM

MD

Henri Mondor University Hospital

Study Sites (1)

Loading locations...

Similar Trials

Portal Hypertension and Liver Resection in... | Clinical Trial