Application of Ultrasound Artificial Intelligence and Elastography in Differential Diagnosis of Breast Nodules

NCT03887598 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2019-03-26

No results posted yet for this study

Summary

The application of computer-aided diagnosis (CAD) technology "S-Detect" enables qualitative and quantitative automated analysis of ultrasound images to obtain objective, repeatable and more accurate diagnostic results. The Elastic Contrast Index (ECI) technique, unlike conventional strain-elastic imaging techniques, can evaluate the elastic distribution in the region of interest. The purpose of the study was to evaluate the differential diagnosis value of ultrasound S-Detect technology for benign and malignant breast nodules and evaluate the differential diagnosis consistency of the ultrasound S-Detect technique and the examiner for benign and malignant breast nodules and explore the differential diagnosis value of Samsung ultrasound elastic contrast Index (ECI) technique for benign and malignant breast nodules.

Conditions

Interventions

DEVICE

Ultrasound diagnosis

Ultrasound diagnosis of lesions with Samsung S-Detect and ECI technology

Sponsors & Collaborators

  • Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

    collaborator OTHER
  • Taizhou Hospital

    collaborator OTHER
  • Wuhan Hospital of Traditional Chinese Medicine

    collaborator OTHER
  • Macheng People's Hospital

    collaborator UNKNOWN
  • Huangshi Central Hospital

    collaborator OTHER
  • Affiliated Hospital of Jiangsu University

    collaborator OTHER
  • The First People's Hospital of Yichang

    collaborator UNKNOWN
  • Yichang Second People's Hospital

    collaborator OTHER
  • Xiangyang Central Hospital

    collaborator OTHER
  • The Second Hospital of Anhui Medical University

    collaborator OTHER
  • Anqing People's Hospital

    collaborator UNKNOWN
  • Huainan People's Hospital

    collaborator UNKNOWN
  • Wenzhou Central Hospital

    collaborator OTHER
  • Xuzhou First People's Hospital

    collaborator UNKNOWN
  • The Central Hospital of Lishui City

    collaborator OTHER
  • Huai'an First People's Hospital

    collaborator OTHER
  • WISCO General Hospital

    collaborator UNKNOWN
  • First People's Hospital of Jiangxia District, Wuhan City

    collaborator UNKNOWN
  • Enshi State Central Hospital

    collaborator UNKNOWN
  • Lianyungang Third People's Hospital

    collaborator UNKNOWN
  • First People's Hospital of Xianyang

    collaborator OTHER
  • Xin-Wu Cui

    lead OTHER

Principal Investigators

  • Xin-Wu Cui, PhD,MD · Tongji Hospital

  • You-Bin Deng, PhD,MD · Tongji Hospital

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-01-18
Primary Completion
2020-01-18
Completion
2020-02-18
FDA Device
Yes

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03887598 on ClinicalTrials.gov