🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT06713915
Starting soon Observational

Diagnostic Performance of Contrast-Enhanced Mammography

NCT06713915 · tracked via the Priya Life Science China tracker
Sponsor
ZHOU Yidong
Phase
Observational
Started
2025-01
Last updated
2024-12-03

Condition(s) studied

Mammography

Investigational drug(s) / intervention(s)

Contrast-Enhanced Mammography

Contrast-Enhanced Mammography: Only patients in the prospective cohort will undergo CEM in addition to breast ultrasound.

Study summary

Contrast-Enhanced Mammography (CEM) is a functional breast imaging technology. Like magnetic resonance imaging (MRI), CEM neovascularization enhancement can improve cancer detection rates, while lack of enhancement may lead to benign determination. The advantages of CEM are dramatically apparent in women with dense breasts. The purpose of this study was to investigate the additional diagnostic value of CEM added to the standard practice of mammography plus ultrasonography(US) in patients with suspicious breast lesions.

This study was a single-center prospective-retrospective combined observational study. In the prospective part, women with suspected breast abnormalities undergo prospective CEM evaluation, including acquisition of low energy (LE) images and recombined images (RI) showing enhancement, concurrently with breast US. The retrospective part selected the mammography and breast US data of female patients with suspected breast abnormalities who had previous baseline matching.

Eligibility

Sex
FEMALE
Min age
30 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Breast ultrasound or/and general mammography suggest that the lesion is BI-RADS 4 or above; * Willing to undergo enhanced mammography examination; * Agree to perform tumor core needle biopsy or excisional biopsy to confirm pathological diagnosis when necessary. Exclusion Criteria: * Allergy to iodinated contrast; * Pregnant and lactating women; * Suffering from kidney disease or abnormal kidney function, or undergoing renal dialysis; * The breast is too large to be completely included in the full-field mammography examination at one time; ○5 Those with breast implants.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Breast Surgery,Peking Union Medical College Hospital Beijing Beijing Municipality
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06713915 on ClinicalTrials.gov ↗ ← All trials in China