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Microwave Ablation for Pulmonary Metastases From Colorectal Cancer

CT-guided Percutaneous Microwave Ablation for Pulmonary Metastases From Colorectal Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02502630
Enrollment
32
Registered
2015-07-20
Start date
2010-06-30
Completion date
2015-07-31
Last updated
2016-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Brief summary

(MWA) is the most recent development in the field of local ablative therapies. The aim of this study was to evaluate CT-guided percutaneous microwave (MW) ablation safety and efficacy in pulmonary metastases from colorectal cancer.

Detailed description

From June 2010 to June 2015, 48 unresectable lesions in 32 patients with pulmonary metastases from colorectal cancer were selected for CT-guided microwave ablation. Patients were scheduled for a 1 and 3 month CT follow-up to evaluate lesion diameter.We retrospectively evaluated CT-guided percutaneous microwave (MW) ablation safety and efficacy in pulmonary metastases from colorectal cancer.

Interventions

DEVICEmicrowave ablation

pulmonary metastases from colorectal cancer are destructed/ablated using microwave ablation

Sponsors

The First People's Hospital of Changzhou
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Unresectable pulmonary metastases from colorectal cancer. * diagnosis by CT, and confirmed by percutaneous puncture biopsy. * Age range 18-70 years old. * Eastern Cooperative Oncology Group performance status 0-1. * Life expectancy of more than 3 months. * Adequate organ function.

Exclusion criteria

* Resectable lung metastases. * Life expectancy less than 3 months * Patients with cardiac pacemaker, cerebral aneurysm clips, implanted electronic instruments or other metal materials. * Coagulopathy with platelet count less than 50000. * Active infectious disease. * Age below 18 years. * Pregnancy of breastfeeding.

Design outcomes

Primary

MeasureTime frame
Overall Survival (OS)one year

Secondary

MeasureTime frame
Treatment related adverse eventsEight weeks

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026