Skip to content

Single-probe Microwave Ablation (MWA) of Metastatic Liver Cancer

Single-probe Microwave Ablation of Metastatic Liver Cancer is Highly Variable and Irreproducible

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00922181
Acronym
LiverMWA1
Enrollment
19
Registered
2009-06-17
Start date
2008-08-31
Completion date
2009-04-30
Last updated
2009-11-16

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

Conditions

Liver Neoplasms

Keywords

malignancy, liver, microwave, surgery

Brief summary

Microwave ablation (MWA) is the most recent development in the field of local ablative therapies. The aim of this study was to evaluate the variability and reproducibility of single-probe MWA versus radiofrequency ablation (RFA) of metastatic liver tumours smaller than 3 cm in patients without underlying liver disease.

Interventions

DEVICEMicrowave ablation

Liver tumors are destructed/ablated using single-probe microwave energy device

DEVICERadiofrequency ablation

Liver tumors are destructed/ablated using radiofrequency energy device

Sponsors

University Hospital, Gasthuisberg
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Unresectable metastatic liver cancer * No invasion of major biliary structures * No invasion of major vascular structures * ASA score \< 4 * WHO score 0-1 * Pre-operative chemotherapy is allowed

Exclusion criteria

* Resectable liver 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
Variability of ablation diameterswithin the first 7 days and 3 months after surgery

Countries

Belgium

Outcome results

None listed

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