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Clinical Trials/NCT02727179
NCT02727179
Completed
Not Applicable

Prospective and Randomized Study Comparing Open vs Laparoscopic Liver Surgery for Colorectal Liver Metastases

Hospital Universitario Virgen de la Arrixaca1 site in 1 country200 target enrollmentFebruary 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colorectal Liver Metastasis
Sponsor
Hospital Universitario Virgen de la Arrixaca
Enrollment
200
Locations
1
Primary Endpoint
Overall survival
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This study evaluates the feasibility of laparoscopic surgery in patients diagnosed with colorectal liver metastases. Half of participants will be operated on by laparoscopic approach and the results obtained will be compared with the results from the other half of patients operated on by open approach.

Detailed Description

The safety and efficacy of liver surgery in the treatment of colorectal liver metastases are well established for the open approach. It allows good results in terms of complications, disease free survival and overall survival, and for these reasons it has become the gold standard technique in the treatment of colorectal liver metastases. On the contrary, the role of laparoscopic liver resection in this context is not so clear nowadays. Generally, laparoscopic surgery offers some advantages such as less pain, shorter hospital stay and better aesthetic results. But the use of laparoscopic approach in liver surgery is still discussing: two international consensus conferences have been held and no strong conclusions have been made. Furthermore for colorectal liver metastases no randomized trials, comparing both techniques, have been published until now. To assess the feasibility of laparoscopic liver resection for colorectal metastases, the investigators propose this trial in which the patients suitable for laparoscopic approach are randomized to open or laparoscopic group

Registry
clinicaltrials.gov
Start Date
February 2005
End Date
March 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital Universitario Virgen de la Arrixaca
Responsible Party
Principal Investigator
Principal Investigator

Ricardo Robles Campos

MD, PHD

Hospital Universitario Virgen de la Arrixaca

Eligibility Criteria

Inclusion Criteria

  • Patients with colorectal liver metastases;
  • Patients suitable for surgical treatment;
  • Patients eligible for laparoscopy approach.

Exclusion Criteria

  • Patients with high tumour load: multiples and bilobar colorectal metastases;
  • Patients with big liver metastases or close to major vessels;
  • Patients with oncological contraindications for surgery;
  • Cirrhotic liver
  • Needing for two stage liver resection;
  • Medical or psychiatric condition of the patient that compromises the informed consent authorization;
  • Refusal to participate in the study

Outcomes

Primary Outcomes

Overall survival

Time Frame: 1 year

Secondary Outcomes

  • Hospital stay(Up to 3 months)
  • Blood losses(Intraoperative)
  • Transfusion(Intraoperative)
  • Mortality(90 days)
  • Morbidity(90 days)
  • Surgical operative time(Intraoperative)
  • Time between surgery and adjuvant chemotherapy(Up to 3 months)

Study Sites (1)

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