Breast Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Women aged 18 years or older
- People who are able to provide written consent to participate
- Women who have recently been diagnosed with breast cancer
- Women who are in the planning stage before surgery and whose tumor is estimated to be 2.0 cm or smaller based on available scans
- Women who are in the planning stage before surgery and who had a breast biopsy at least 10 days before the special scan used in this trial
Who may not be able to join:
- People who have a reason they cannot safely have an MRI scan, including having an electronic implant such as a pacemaker, having a metal implant such as an aneurysm clip, having claustrophobia (fear of enclosed spaces), or having kidney failure severe enough that the contrast dye used in MRI scans is considered unsafe by FDA guidance (confirm with trial site)
- Women who are pregnant
- Women who have breast implants
- People who are currently imprisoned
- People whose breast biopsy site has not healed well enough to be visually acceptable
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Keith D. Paulsen, PhD, Dartmouth College
Phone: 603-646-2695
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Optical sensitivity of the MRg-NIRS platform
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.