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Recruiting NCT06353672

A Study to Evaluate Safety and Feasibility of Robotic Liver Resection

No phase Interventional Liver Diseases Surgery

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Robotic liver resection.
Who it may be relevant to
Registry conditions: Liver Diseases, Surgery. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The robotic surgery system, the most advanced technology in minimally invasive surgery, overcame some shortcomings of laparoscopic surgery and improved the flexibility and precision of liver resection. Several studies have demonstrated that the robotic system was safe and feasible in liver surgery and might be advantageous in complex hepatic vein and hilar dissection, operative bleeding control, and biliary reconstruction. Previous comparative studies found limited evidence for significantly improved outcomes in robotic liver resection (RLR) over laparoscopic liver resection (LLR) or open liver resection (OLR), considering the various degrees of difficulty in liver surgeries. This study aimed to evaluate safety and feasibility of robotic liver resection, by comparing it with LLR or OLR, and gain veritable and relevant data on the benefits of RLR.

Interventions

  • Device Robotic liver resection
    Liver resection using Da Vinci robotic system

Primary outcome measures

  • Postoperative complications [Time frame: with in 90 days after surgery]
  • Postoperative hospital stay [Time frame: with in 90 days after surgery]
  • Postoperative unplanned reoperation [Time frame: with in 90 days after surgery]
  • Unplanned readmission [Time frame: with in 90 days after surgery]

Eligibility criteria

Inclusion criteria

  • The patients were diagnosed with a liver tumor.
  • The patients underwent robotic liver resection.

Exclusion criteria

  • The patients underwent simultaneous malignancy resection of the colorectum or other organs (except gallbladder).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

China · 1 center
  • First Affiliated Hospital, Medical College of Zhejiang University — Hangzhou

Identifiers

NCT: NCT06353672 · RLR-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗