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Clinical Trials/NCT05273489
NCT05273489CompletedNot Applicable

Effect of Chemotherapy and Tumor Clearance in Hepatic Resections for Colorectal Liver Metastases. A Single-centre Cohort Study

Hospital Maciel0 sites170 target enrollmentStarted: January 1, 2004Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
170
Primary Endpoint
Survival

Study Overview

Brief Summary

Retrospective analysis of a prospectively collected database of 170 patients between 2004 and 2020, who underwent liver resections for CRLM (colorectal liver metastases) at The Queen Elizabeth Hospital trying to determine rates and patterns of recurrence following liver resections for CRLM and concurrently, characterise clinical, pathological and treatment-related factors that could function as predictors of recurrence or survival, particularly neoadjuvant chemotherapy and tumour clearance.

Detailed Description

This is a descriptive, observational study with retrospective analysis of a prospectively collated database. This database included all patients who underwent curative hepatic resections for CRLM (colorectal liver metastases) at The Queen Elizabeth Hospital (Adelaide, Australia) between December 2004 and October 2020.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Other

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients who underwent a liver resection for CRLM at The Queen Elizabeth Hospital between December 2004 to September 2020

Exclusion Criteria

  • Patients whose procedures were abandoned due to unresectable tumour burden

Outcomes

Primary Outcomes

Survival

Time Frame: From surgery to death or end of the study, up to 16 years

up to16 years

Recurrence

Time Frame: From surgery to recurrence, up to 16 years

Recurrence rate

Secondary Outcomes

  • Resection margins(From surgery to death or end of the study, up to 16 years)
  • Neoadjuvant Chemotherapy(From surgery to death or end of the study, up to 16 years)

Investigators

Sponsor
Hospital Maciel
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mauro Andres Perdomo, MD, MHA

MD, General Surgeon

Hospital Maciel

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