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Preliminary Study of Microwave Tumoral Ablation Performances for the Treatment of Pulmonary, Renal and Bone Neoplasia.

Preliminary Study of Microwave Tumoral Ablation Performances for the Treatment of Pulmonary, Renal and Bone Neoplasia.

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02862288
Acronym
TherMO
Enrollment
30
Registered
2016-08-11
Start date
2012-09-30
Completion date
2015-12-31
Last updated
2016-08-11

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

Conditions

Bone Tumor, Lung Tumor, Renal Tumor

Brief summary

The aims of this work were to assess the feasibility, efficacy, short-term outcome and safety of microwave ablation in the treatment of malignant bone, lung and renal tumors.

Interventions

DEVICEMicrowave ablation with Acculis Accu2i pMTA Applicator

Sponsors

Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Men and women \> 18 years old * Thermoablation indication of renal neoplasia, bone or lung decided during a multidisciplinary consultation meeting - Generally speaking, the indications are: (i) inoperable primary malignant tumor or secondary malignant tumor, (ii) resectable primary malignant renal and lung tumor with medical contraindication to surgery or general anesthesia * Signature of informed consent for participation * Affiliation to a social security scheme or French beneficiary of such a regime.

Exclusion criteria

* Contraindication to percutaneous thermoablation * Renal or lung tumor up to 4 cm * Women of childbearing age, premenopausal, non-sterilized surgically, and unwilling to use effective contraception * Legal incapacity or legal capacity limited * Person unlikely to cooperate in the study and / or low degree of cooperation expected by the investigator * Person without health insurance * Pregnant women

Design outcomes

Primary

MeasureTime frame
Tumor necrosis rate in post-intervention over one month monitoring period.one month

Countries

France

Outcome results

None listed

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