Gradient-Echo Spectroscopic Imaging Study of Saturated Fat and Breast Cancer
NCT ID: NCT03400215
Last Updated: 2025-04-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
135 participants
INTERVENTIONAL
2018-07-23
2025-04-17
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Positron Emission Tomography Before Surgery in Evaluating Women With Primary or Recurrent Breast Cancer
NCT00039286
Breast Density and the Role of Preoperative Mammography, Ultrasound, Elastography and MRI
NCT00695968
Evaluate The Accuracy Of Breast MRI Biopsy In Diagnosing A Complete Tumor Response For Some Women Following Neoadjuvant Chemotherapy For Breast Cancer
NCT03289195
Extent of Breast Cancer and the Role of Pre-Operative Sonography and MRI
NCT02587663
3.0 Tesla Magnetic Resonance Imaging for Breast Cancer Detection in High Risk Women
NCT01409226
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Breast cancer confirmed by biopsy
Cases will be women first diagnosed with invasive breast cancer confirmed by biopsy
Diagnostic Breast Cancer Scan
clinically indicated diagnostic breast MRI scans
Research Scan for Gradient-echo Spectroscopic Imaging (GSI)
15-min research MRI scan
Women without any history of breast cancer
No known malignancy confirmed by at least 1-year follow up exams.
Diagnostic Breast Cancer Scan
clinically indicated diagnostic breast MRI scans
Research Scan for Gradient-echo Spectroscopic Imaging (GSI)
15-min research MRI scan
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Diagnostic Breast Cancer Scan
clinically indicated diagnostic breast MRI scans
Research Scan for Gradient-echo Spectroscopic Imaging (GSI)
15-min research MRI scan
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No contraindication to gadolinium contrast agent (severe renal insufficiency (EGFR\<30), allergy to gadolinium) which will be injected for clinical exam
* Able and willing to provide informed consent
* Post-menopausal age \> 25 years.
Exclusion Criteria
* Breast surgery within prior 12 months, or breast implants
* Any hormonal therapy
25 Years
99 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
NYU Langone Health
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Linda Moy, MD
Role: PRINCIPAL_INVESTIGATOR
NYU Langone Health
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
NYU Langone Health
New York, New York, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
17-01549
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.