๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2014-06-24

Intensity Modulated Radiotherapy (IMRT) vs. 3D-conformal Accelerated Partial Breast Irradiation (APBI) for Early Stage Breast Cancer After Lumpectomy (NCT01185132)

A Phase III Randomized Study Comparing Intensity Modulated Planning Versus 3-Dimensional Planning for Accelerated Partial Breast Radiotherapy

๐ŸŸข Recruiting Phase3 ๐Ÿ“‹ Clinical Research Protocol Sponsor: Rocky Mountain Cancer Centers

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

In the setting of radiotherapy as part of breast-conservation therapy for patients with early stage breast cancer, the novel planning and delivery method of intensity modulated radiotherapy is an effective and safe alternative to the commonly-used standard 3D-conformal external beam radiotherapy, spares more normal breast and lung tissue, and may lead to improved clinical outcomes.

Who can join: Review the eligibility criteria below.

Location: Rocky Mountain Cancer Centers - Aurora โ€” Aurora, Colorado

Age range: 40 Years

๐Ÿงช Interventions in This Study

  • accelerated partial breast irradiation - 3D-conformal planning (RADIATION)
  • accelerated partial breast irradiation - IMRT planning (RADIATION)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

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

๐Ÿ“ All Participating Trial Locations (5 Sites)

  • Rocky Mountain Cancer Centers - Aurora โ€” Aurora, Colorado
  • Rocky Mountain Cancer Centers - Boulder โ€” Boulder, Colorado
  • Rocky Mountain Cancer Centers - Lakewood โ€” Lakewood, Colorado
  • Rocky Mountain Cancer Centers - Littleton โ€” Littleton, Colorado
  • Rocky Mountain Cancer Centers - Thornton โ€” Thornton, Colorado

๐Ÿ“ž Contact the Study Coordinator

Phone: (303) 418-7607

Email: rachel.lei@usoncology.com

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

๐Ÿ’ฐ 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 ยง 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 Cancer clinical trials

๐Ÿ’ก 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.
๐Ÿ›๏ธ View Official NIH Record โ†—