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Clinical multicenter study on ultrasound identification and risk stratification management of breast papillary tumors

Clinical multicenter study on ultrasound identification and risk stratification management of breast papillary tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100871
Enrollment
Unknown
Registered
2025-04-16
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Papillary tumor

Interventions

Gold Standard:Minimally invasive or surgical pathology results
Index test:Multi-parameter ultrasound examination parameters(grayscale ultrasound, color Doppler imaging, MV Flow imaging, and elastography)

Sponsors

Affiliated hangzhou first people's hospital, zhejiang university school of medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age ranged from 18 to 80 years old, with independent behavioral ability, voluntarily participating in this study and signing an informed consent fo; 2.Spontaneous or pathological nipple discharge detected during physical examination (excluding milk like and clear water like colors); 3.Breast ultrasound examination shows ductal related masses, mixed cystic and solid masses, debris in expanded catheter,Isolated nodules with clear margin and abundant blood supply; 4.Other imaging examinations suspect intraductal tumors; 5.The final result is confirmed by minimally invasive or surgical pathology, and the interval between the last preoperative ultrasound examination and resection is less than 3 months;

Exclusion criteria

Exclusion criteria: 1.Patients during lactation and pregnancy; 2.Patients with ipsilateral breast surgery history or recent radiotherapy of breast cancer; 3.Individuals with incomplete case data or images that are not up to standard; 4.Patients whose lesions cannot be clearly displayed by ultrasound;

Design outcomes

Primary

MeasureTime frame
Positive predictive value;sensitivity;specificity;

Countries

China

Contacts

Public ContactLingyun Bao

Affiliated hangzhou first people's hospital, zhejiang university school of medicine

hzs1bly@zju.edu.cn+86 571 56007130

Outcome results

None listed

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