MRg-NIRS Imaging for Breast Cancer

MRg-NIRS Imaging System Breast Cancer Trial

Recruiting N/A Interventional Study
Breast Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 83
Sex
Female
Study type
Interventional
Purpose
Device Feasibility
Participants needed
20 (estimated)
Sponsor
Keith D. Paulsen · Other
Who this trial is looking for

This trial is looking for women with breast cancer to see how a new imaging method can help in their treatment. Participants will receive MR-guided near-infrared imaging along with standard care.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am a female aged 18 or older
  • I can provide written consent
  • I have a recent diagnosis of breast cancer
  • I have an estimated tumor size of 2.0 cm or less
  • I had a breast biopsy at least 10 days before the exam

You may not be able to join if

  • I have an electronic implant like a pacemaker
  • I have a metal implant like an aneurysm clip
  • I have claustrophobia
  • I have kidney failure
  • I am pregnant
  • I have breast implants
  • I am a prisoner
  • I have not healed properly from a breast biopsy

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial

This trial is a study of 20 women with breast cancer to evaluate the addition of MR-guided (MRg) near-infrared spectroscopy (NIRS) with and without contrast, as part of a program to improve clinical management of women receiving breast magnetic resonance imaging (MRI).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Females age ≥ 18 years old 2. Participants capable of providing written informed consent 3. Women with a recent diagnosis of breast cancer. 4. Women who are in pre-surgical planning must have an estimated tumor size of 2.0 cm or less on available imaging. 5. Women who are in …
Contacts

Keith D. Paulsen, PhD

603-646-2695

Keith.D.Paulsen@Dartmouth.edu

CONTACT

Shudong Jiang, PhD

Shudong.Jiang@Dartmouth.edu

CONTACT