Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Clinical diagnosis of breast cancer
- Age between 18 and 80 years
You will not qualify if you...
- Missing pathology data
- Missing follow-up results
- Missing data
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
Actively Recruiting
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
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here