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Prognostic Impact of Anatomical Resection Vs. Non-anatomical Resection for HCC

Anatomical Liver Resection by Means of Ultrasound-guided Vessel Compression Versus Non-anatomical Resection for Hepatocellular Carcinoma: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01236989
Acronym
ARversusNAR
Enrollment
120
Registered
2010-11-09
Start date
2011-01-31
Completion date
2017-12-31
Last updated
2010-11-09

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

Conditions

Disease-Free Survival, Overall Survival, Patients Affected by Hepatocellular Carcinoma

Keywords

anatomical resection, non-anatomical resection, IOUS-guided finger compression

Brief summary

Prognostic impact of AR vs NAR

Detailed description

Whether anatomical is better than non anatomical resection for HCC is still debated. This prospective randomized study aimed to address which approach is better in terms of patients prognosis.

Interventions

anatomical liver resection by means of IOUS-finger compression

PROCEDURENon-anatomical liver resection

non-anatomical liver resection

Sponsors

University of Milan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patient affected by single HCC * patients in whom liver resection is indicated * HCC without vascular invasion and/or thrombosis

Exclusion criteria

* multinodular HCC * metastatic disease * spontaneous tumor rupture

Design outcomes

Primary

MeasureTime frame
the prognostic impact of anatomical resection by means of intraoperative ultrasound (IOUS) guided vessel compression versus nonanatomical resection in terms of disease free and overall survival5-years

Secondary

MeasureTime frame
the impact of anatomical resection versus non-anatomical resection in terms of postoperative mortality and morbility30 and 90 days

Countries

Italy

Contacts

Primary ContactGuido Torzilli, MD, PhD
guido.torzilli@unimi.it+39 02 8224

Outcome results

None listed

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