Variability of Microwave Ablation Volume Based on Clinical, Radiological, Biological, and Tissue Factors
Condition(s) studied
Study summary
Microwave ablation is a minimally invasive technique whose planning relies on manufacturer tables derived from ex vivo models that do not account for patient or tumor-specific factors. In clinical practice, the actual ablation volume often differs from the planned volume due to liver characteristics, vascular proximity, and tumor biology.
This study aims to assess the variability between ablation small axis during percutaneous microwave ablation of liver lesions. The influence of patient-related (fibrosis, steatosis, portal flow) and tumor-related factors (location, histology, prior treatment) will be evaluated. Small axis and volume will be compared with volumes measured on immediate post-procedural CT and on CT/MRI at 6-12 weeks, accounting for expected tissue shrinkage.
Eligibility
Primary outcome measure(s)
- Small final ablation axis measured on the post-procedure imaging modality considered to be the most reliable. — 12 weeks
The final short axis will preferably be measured (in mm) on MRI at 6-12 weeks. If inter-patient variability in volume shrinkage exceeds 5%, the modality with the lowest relative variability (usually the immediate CT scan) will be used as the reference for estimating the final volume.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| CHRU Nancy | Vandœuvre-lès-Nancy | France | Recruiting |
More Central Hospital, Nancy, France trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07413640 on ClinicalTrials.gov ↗ ← All trials in France