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A Study of Breast Cancer Risk Factors and Outcomes of People in Florida

Genomic and Non-Genomic Factors Associated With Breast Cancer Risk Factors and Outcomes in a Diverse South Florida Population

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06780176
Enrollment
800
Registered
2025-01-17
Start date
2025-01-13
Completion date
2030-01-13
Last updated
2026-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Breast Diseases, Breast Neoplasms

Keywords

breast cancer, breast neoplasms, breast diseases, BIRADS, Memorial Sloan Kettering Cancer Center, 24-372

Brief summary

The purpose of this study is to understand why different people have different risks and outcomes for breast cancer and non-breast cancer.

Interventions

OTHERBiospecimen Collection

Blood collection at baseline and time of surgery

DIAGNOSTIC_TESTSurgical Tissue Collection

Tissue collection will be attempted at time of surgery

BEHAVIORALSurvey Collection

Survey collection at baseline, post-surgery, at 1, 3 and 5 year follow up visits

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients with BIRADS 0-5, seen in breast radiology clinic at University of Miami (UM), Sylvester Comprehensive Cancer Center (SCCC), Jackson Health Systems (JHS) for biopsy. * Any new breast patient seen at UM/SCCC or JHS will be invited to participate in the study. * Men and women 18 years of age and older are eligible to participate in the study.

Exclusion criteria

* Patients who are less than 18 years of age will be considered ineligible. * Patients unable to complete the survey.

Design outcomes

Primary

MeasureTime frameDescription
Clinical characteristic of participants (survey)Up to 5 yearsThe purpose of this study is to prospectively collect and store clinical data, blood and tissue samples, and participant survey data to evaluate (epi) genomic and non-genomic causes of disparity.

Countries

United States

Contacts

CONTACTNeha Goel, MD, MPH
goeln1@mskcc.org646-888-4731
CONTACTGeorge Plitas, MD
plitasg@mskcc.org646-888-5368
PRINCIPAL_INVESTIGATORNeha Goel, MD, MPH

Memorial Sloan Kettering Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026