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Magnetic Resonance Imaging of Breast Cancer

Magnetic Resonance Imaging of Breast Cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01035112
Enrollment
500
Registered
2009-12-18
Start date
1995-04-01
Completion date
2027-05-01
Last updated
2026-07-01

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

Conditions

Breast Cancer, Breast Cancer Non-invasive Breast Cancer

Brief summary

To compare magnetic resonance imaging (MRI) with more well established diagnostic imaging techniques to determine which method best finds and defines breast cancer.

Interventions

PROCEDUREMRI

Sponsors

Stanford University
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH
National Institutes of Health (NIH)
CollaboratorNIH
National Institute for Biomedical Imaging and Bioengineering (NIBIB)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Female * Documented breast physical examination, * Documented mammography within 3 months of the MR studies * Palpable or mammographically-detected suspect breast lesions * Women who have already undergone lumpectomy for breast cancer and have post-biopsy/post-radiation changes will be eligible if they have mammographically-detected or palpable breast abnormalities which are sufficiently suspicious to merit core needle or surgical biopsy.

Exclusion criteria

* Male by birth * Able to complete the MR examination. Subjects will be interviewed by one of the investigators for the usual contraindications to * MR contraindications including * Pacemakers * Metallic implants * Severe claustrophobia * Aneurysm clips * Pregnancy * Current lactation * Other conditions precluding proximity to a strong magnetic field. * Received an enhanced MR procedure within 48 hours, * Iodinated contrast within six hours, * Known sensitivity to MR contrast agents, * Not likely to complete the study in full or * Other clinical reason which would preclude participation in the protocol.

Design outcomes

Primary

MeasureTime frame
To compare magnetic resonance imaging (MRI) with more well established diagnostic imaging techniques to determine which method best finds and defines breast cancer.Length of one MRI scan

Countries

United States

Contacts

CONTACTJocelyn Steffan
jsteffen@stanford.edu650-725-1812
PRINCIPAL_INVESTIGATORBruce L Daniel

Stanford University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 2, 2026