Clinical trial · Observational
Microwave Ablation of Breast Tumors
NCT04828044CI-TRIAL-00050995withdrawnClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Lack of sufficient funding
Summary
Brief summary (as posted)
The purpose of this protocol is to pathologically evaluate the amount of destruction of cancer cells by Microwave Ablation (MWA) in primary breast tumors.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Microwave Ablation/ Coagulation Arm | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Microwave Ablation/ Coagulation Arm
- description
- These patients will receive microwave ablation using MedWaves Microwave Ablation/ Coagulation System.
- interventionNames
- Device: Microwave Ablation/ Coagulation Arm
Primary outcomes (1)
- measure
- Amount of tissue destruction with MedWaves Microwave Ablation/ Coagulation System.
- timeFrame
- 30 days
- description
- Measure tissue destruction with the MedWaves Microwave Ablation/ Coagulation System through pathological review of destruction.
Secondary outcomes (2)
- measure
- Provide the differences between percutaneous and open Microwave Ablation
- timeFrame
- 30 Days
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 90 Years
Show eligibility criteria text
Inclusion Criteria: * a diagnosis of primary breast tumor for which a surgical resection (excisional, biopsy, segmentectomy or mastectomy) is planned. * Tumor is palpable or visible on ultrasound or both * All participants need to be fully able to give informed consent Exclusion Criteria: * Gender: male * Mental or legal incompetence * Impaired decision-making capacity * Pregnant women may not participate * Implanted Pacemaker
References
Publications (0)
Data not yet available
No reference posted for this study.