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Percutaneous microwave ablation of small breast cancer

Percutaneous microwave ablation of small breast cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000029155
Enrollment
Unknown
Registered
2020-01-16
Start date
2020-02-01
Completion date
Unknown
Last updated
2020-01-20

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

Conditions

breast cancer

Interventions

Sponsors

The First Affiliated Hospital, Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Female, older than 18 years; 2. Pathological diagnosis of breast cancer by thick needle puncture without distant metastasis; 3. B-ultrasound or molybdenum target confirmed as a single breast neoplasm with no suspected dispersed intraductal cancer components; 4. The diameter of the tumor measured by B-ultrasound in the supine position less than 3 cm. The distance of the tumor from chest wall, nipple and skin more than 0.5 cm; 5. Karnofsky score >= 70%; 6. Informed consent.

Exclusion criteria

Exclusion criteria: 1. Evidence of extensive intraductal carcinogenesis in invasive breast cancer; 2. Multifocal breast tumors; 3. Duration of pregnancy or lactation; 4. Patients with coagulative disease, chronic liver disease or renal failure; 5. HIV infection or the presence of AIDS-related diseases, or severe acute and chronic diseases; 6. Severe active infections (>grade 2, NCI-CTCAE 3.0); 7. People with low compliance assessed by researchers; 8. Epilepsy patients requiring medication (e.g. steroids or antiepileptic drugs); 9. Psychological or psychiatric disorders such as drug abuse or the possibility that patients may interfere with research compliance; 10. receiving systemic chemotherapy, targeted drug therapy or local radiotherapy; 11. Any situation that is unstable or may endanger the safety and compliance of patients in this study.

Design outcomes

Primary

MeasureTime frame
complete ablation rate;

Secondary

MeasureTime frame
disease-freesurvival, DFS;overallsurvival, OS;T cell;NK cell;Immune cells;

Countries

China

Contacts

Public ContactShui Wang

The First Affiliated Hospital, Nanjing Medical University

ws0801@hotmail.com+86 13701458115

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026