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Recruiting NCT06698146

Colorectal Metastasis to Liver Extraction With Auxiliary Transplant and Delayed Resection

Observational Liver Transplant Surgery Colorectal Cancer Metastatic Colon Cancer Liver Metastases

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Liver Transplant Surgery, Colorectal Cancer Metastatic, Colon Cancer Liver Metastases. Basic parameters: from 18 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
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Colorectal Metastasis to Liver Extraction With Auxiliary Transplant and Delayed Resection Registry Study

Overview

Liver transplantation (LT) has become an accepted treatment for selected patients with unresectable liver metastases due to colorectal cancer (CRLM). The goal of this study is to look at and compare the clinical results of all the different approved methods (living vs. Deceased, whole organ vs. Split, one staged vs. Two staged) used to perform a standard liver transplant procedure for recipients with CRLM. Investigators will look at things like different procedure results, recovery in the hospital, and survival rates one year after the transplant. Investigators will also take blood samples from participants to be used in future research. All the transplant methods the investigators are comparing are standard practices approved by the United Network of Organ Sharing (UNOS).

Primary outcome measures

  • Graft and Patient Survival Outcomes [Time frame: From liver transplant to 12 months]
Secondary outcome measures (1)
  • Outcomes of liver transplant recipients [Time frame: From liver transplant to 12 months]

Eligibility criteria

Inclusion:

  • All Patients of either gender ≥ 18 years of age who are listed for Liver transplant candidates at Northwestern with liver metastases due to colorectal cancer (CRLM).
  • Subjects must be able to provide informed consent themselves and without the use of a legally authorized representative (LAR), to be determined by the PI or Sub-I at the time of Consent.

Exclusion:

  • Adults unable to consent
  • Pregnant Women
  • Certain clinical/surgical/anatomical parameters, at the discretion of the PI.

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

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 1 center
  • Northwestern University-Comprehensive Transplant Center — Chicago

Identifiers

NCT: NCT06698146 · STU00222933

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗