Status:

UNKNOWN

Independent Risk Factors Analysis and Model Construction For Recurrence After Radiofrequency/Microwave Ablation of Colorectal Cancer With Liver Metastases: a Retrospective, Multicenter Trial

Lead Sponsor:

The Central Hospital of Lishui City

Collaborating Sponsors:

Zhejiang Cancer Hospital

Zhejiang University

Conditions:

Colorectal Cancer With Liver Metastases

Eligibility:

All Genders

18+ years

Brief Summary

This study is a retrospective, multicenter clinical study. The main objective is to analyze the risk factors affecting the recurrence of colorectal cancer patients with liver metastases who received r...

Eligibility Criteria

Inclusion

  • Age:older than 18 years;
  • Patients with a single tumor diameter ≤5cm, no more than 3 tumor nodules, and the largest tumor diameter ≤3cm;
  • Absence of vessel, bile duct and adjacent organ invasion and distant metastasis;
  • The primary tumor of colorectal cancer has been resected, the liver metastases cannot be resected or the patient is unwilling to undergo surgery (clinical or pathological confirmation);
  • Normal coagulation status and liver function child-pugh A or B;
  • Liver metastases have not received other antitumor therapy after radiofrequency/microwave therapy (before disease progression);
  • Routine laboratory tests were performed before the first RF/microwave treatment;
  • Follow up for more than 12 months;
  • Obtained free informed consent.

Exclusion

  • Large tumor, or diffuse intrahepatic metastasis;
  • Accompanied by vascular tumor thrombus or invasion of adjacent organs;
  • The primary tumor of colorectal cancer has not been resected, with extrahepatic metastasis;
  • Uncorrectable coagulation dysfunction and severe blood abnormalities, those with severe bleeding tendency;
  • Intractable massive ascites, cachexia;
  • Active infection, especially inflammation of the biliary system;
  • Severe liver, kidney, heart, lung, brain and other major organ failure;
  • Patients with impaired consciousness or unable to cooperate with treatment;
  • Missing follow-up data.

Key Trial Info

Start Date :

March 12 2022

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

August 12 2022

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT05268549

Start Date

March 12 2022

End Date

August 12 2022

Last Update

March 7 2022

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