None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: -Patients with lesions of BI-RADS category C4b or higher identified through mammography or ultrasound. -Women over 19 Patients with no history of other cancers, including breast cancer Patients who voluntarily decided to participate in this clinical study and signed written informed consent Patients in BI-RADS category C1-2
Exclusion criteria
Exclusion criteria: -Patients with recurrent breast cancer Patients diagnosed with cancer in other organs within 5 years -Patients with other cancers identified by metastases -General condition that prevents you from understanding and submitting consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sensitivity;Specificity | — |
Secondary
| Measure | Time frame |
|---|---|
| Predictive values;Positive predictive values;Negative predictive values;Accuracy | — |
Countries
Korea, Republic of
Contacts
Seoul National University Healthcare System Gangnam Center