LIVACOR Trial: Minimally Invasive LIVer And Simultaneous COlorectal Resection

NCT05138094 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2022-07-25

No results posted yet for this study

Summary

The LIVACOR - Trial is a European wide, randomized controlled, open-label, multicenter trial. Patients with synchronous colorectal liver metastases (CRLMs) and primary colorectal tumor are considered eligible and will be randomized between minimally invasive (MI) combined or staged colorectal resection (all colectomies, including high anterior resection) and liver resection of up to three segments.

Conditions

  • Colorectal Neoplasms Malignant
  • Neoplasm Metastasis

Interventions

PROCEDURE

Minimally invasive simultaneous resection

One minimally invasive surgical procedure wherein both the primary colorectal carcinoma and the liver metastases are removed.

PROCEDURE

Minimally invasive two-stage resection

Two minimally invasive surgical procedures wherein the primary colorectal carcinoma and the liver metastases are removed

Sponsors & Collaborators

  • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

    collaborator OTHER
  • University Hospital Southampton NHS Foundation Trust

    collaborator OTHER
  • University Hospital Birmingham NHS Foundation Trust

    collaborator OTHER
  • Liverpool University Hospitals NHS Foundation Trust

    collaborator OTHER_GOV
  • King's College Hospital NHS Trust

    collaborator OTHER
  • Manchester University NHS Foundation Trust

    collaborator OTHER_GOV
  • Newcastle-upon-Tyne Hospitals NHS Trust

    collaborator OTHER
  • University Hospital Plymouth NHS Trust

    collaborator OTHER
  • Mauriziano Umberto I Hospital

    collaborator OTHER
  • University Hospital Padova

    collaborator OTHER
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

    collaborator OTHER
  • San Raffaele University Hospital, Italy

    collaborator OTHER
  • Ospedali Riuniti Ancona

    collaborator OTHER
  • Azienda Usl di Bologna

    collaborator OTHER_GOV
  • Azienda Ospedaliero-Universitaria di Modena

    collaborator OTHER
  • Federico II University

    collaborator OTHER
  • Parma University Hospital

    collaborator OTHER
  • Klinikum Saarbrücken, Klinik für Allgemein-, Viszeral- und Thoraxchirurgie, Chirurgische Onkologie

    collaborator OTHER
  • Maastricht University Medical Center

    collaborator OTHER
  • University of Navarrra Hospital (Clinica Universitaria)

    collaborator OTHER
  • Hospital del Mar

    collaborator OTHER
  • Assistance Publique - Hôpitaux de Paris

    collaborator OTHER
  • Oslo University Hospital

    collaborator OTHER
  • Ziekenhuis Oost-Limburg

    collaborator OTHER
  • General Hospital Groeninge

    collaborator OTHER
  • Moscow Clinical Scientific Center

    collaborator OTHER
  • Centre Hospitalier du Luxembourg

    collaborator OTHER
  • Fondazione Poliambulanza Istituto Ospedaliero

    lead OTHER

Principal Investigators

  • Professor Mohammed Abu Hilal, MD PhD · Fondazione Poliambulanza Istituto Ospedaliero

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-06
Primary Completion
2023-09-01
Completion
2024-09-01

Countries

  • Belgium
  • France
  • Germany
  • Italy
  • Luxembourg
  • Netherlands
  • Norway
  • Russia
  • Spain
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05138094 on ClinicalTrials.gov