Actively Recruiting

Age: 18Years - 80Years
All Genders
ID04483804

Application of Radiomics in Correlation Between Ultrasound Characteristics and Pathological Prognostic Factors in Breast Cancer

Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2023-03-10

2000

Participants Needed

1

Research Sites

261 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are exploring the relationship between ultrasound features, including conventional ultrasound, elastography, and contrast-enhanced ultrasound (CEUS), and pathological prognostic factors in breast cancer. This observational study uses radiomics, a method that extracts detailed imaging information, to better understand these correlations and their potential clinical relevance. The study is sponsored by the Second Affiliated Hospital, School of Medicine, Zhejiang University, and aims to provide insights into breast cancer prognosis. Participants undergo ultrasound imaging assessments, including advanced techniques like elastography and CEUS, alongside standard pathological evaluations. The study observes patients over an average follow-up period of one year to monitor outcomes such as metastasis and death related to breast cancer progression. While endocrine therapy is noted as an intervention, the study primarily focuses on imaging and pathological data rather than treatment comparison. During the study, participants' ultrasound characteristics and pathological findings are recorded and analyzed using radiomics technology. Researchers track disease-free survival and non-disease-free survival times, noting the time to relapse, metastasis, or death due to disease progression. Data collection includes follow-up results and pathology reports to ensure comprehensive monitoring. The total participation duration aligns with the one-year average follow-up to assess primary outcomes accurately.

CONDITIONS

Brief Title

Application of Radiomics in Breast Cancer

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of breast cancer
  • Age between 18 and 80 years
Not Eligible

You will not qualify if you...

  • Missing pathology data
  • Missing follow-up results
  • Missing data

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Approximately 1 year

Participants are observed to track the progression of breast cancer and outcomes over time.

Periodic visits during the study period

Trial Site Locations

Total: 1 location

1

the Second Affiliated Hospital Zhejiang University School of Medicine

Hanzhou, Zhejiang, China, 310009

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Research Team

Z

zimei Lin

J

jifan Chen

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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