πŸ›οΈ Verified NIH Record β€’ Updated 2025-09-29

Molecular Breast Imaging Guidance for Breast Biopsy for Patients With Breast Abnormalities (NCT06058650)

Pilot Clinical Study to Evaluate Molecular Breast Imaging- Guidance for Sampling of Breast Abnormalities

🟒 Recruiting Observational / Diagnostic 🩺 Clinical Procedure Protocol Sponsor: Mayo Clinic

🩺 Plain-English Summary (8th-Grade Level)

This clinical trial tests how well molecular breast imaging (MBI) works to guide the collection of a breast biopsy in patients with a breast abnormality. Currently, a biopsy is often guided by either ultrasound or mammography in order to ensure that a sample of the correct part of the breast is taken. Sometimes a lesion or part of the lesion cannot be seen on ultrasound or mammography, and, therefore, a biopsy guided with ultrasound or mammography may not be always be accurate. Studies have shown that high resolution MBI may have potential to improve the detection of some breast tumors. This trial uses a new high-resolution MBI system that may help perform a biopsy using MBI.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic in Rochester β€” Rochester, Minnesota

Age range: 18 Years

πŸ§ͺ Interventions in This Study

  • Biopsy of Breast (PROCEDURE)
  • Medical Device Usage and Evaluation (OTHER)
  • Scintimammography (RADIATION)
  • Technetium Tc-99m Sestamibi (OTHER)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (1 Sites)

  • Mayo Clinic in Rochester β€” Rochester, Minnesota

πŸ“ž Contact the Study Coordinator

Phone: (855) 776-0015

Email: mayocliniccancerstudies@mayo.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Breast Neoplasm clinical trials

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—