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A Multi-Modality Surveillance Program for Women at High Risk for Breast Cancer

NCT03729115

This study is recruiting at 3 US sites in 2 states, according to its ClinicalTrials.gov record last updated .

Summary

This study is aimed to establish a registry of women undergoing intensive surveillance for the early detection of breast cancer in high-risk women.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Breast Cancer

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
25 years and older
Sex
Female
Healthy volunteers
Accepted
Sponsor
University of Chicago
Last updated on ClinicalTrials.gov
September 1, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 2

  • University of California, San Diego · La Jolla, CA
  • University of California, Davis · Sacramento, CA

Illinois · 1

  • University Of Chicago Medicine Comprehensive Cancer Center · Chicago, IL

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.