Surveillance MRI Registry for Patients Who Had Breast Cancer With Dense Breast Tissue

Part of paid clinical trials in Houston, Texas.

Sponsor
M.D. Anderson Cancer Center
Study ID
NCT06127797
Status
Recruiting
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Conditions

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Questionnaire/Interview — BEHAVIORAL
    Participation on this study will be over as soon as you complete the questionnaire/interview after your scheduled scans.

Study Details

To create a registry (database) of participants who come in for breast MRI scans. Researchers want to use this information to study if participants with dense breast tissue (tissue that is more difficult to see on mammogram).

Key Dates

Start date
Jan 11, 2024
Status verified
Feb 2026
Primary completion
Aug 31, 2027
Completion
Aug 31, 2029

Study Design

Enrollment
1,000 participants (estimated)

Arms

  • Arm: Questionnaire/Interview
    Participants will take part in this study, before and after your routine breast MRI scan, participants will be asked to answer a series of questions about your experience with this MRI. It may take 10 to 20 minutes to answer. Participants may answer these questions in 1 of 3 ways: * In-person in the clinic with the study team (either through speaking or writing down your answers on a paper or electronic questionnaire form); * by phone at a later time; or * by paper or email at a later time.

Primary Outcome Measure

Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0 [ Time Frame: through study completion; an average of 1 year ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
MD Anderson Cancer CenterHoustonTexas77030
Huong Le-Petross, MD
[email protected]

Find similar trials in Houston, TX

By condition
Breast cancer
By specialty
OncologyBreast oncologyWomen's health
By research site
MD Anderson Cancer Center· Houston, TX

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