A Randomized Trial of Five Fraction Partial Breast Irradiation (RAPID2) (NCT05417516)
A Randomized Trial of Five-Fraction Partial Breast Irradiation (RAPID2)
π©Ί Plain-English Summary (8th-Grade Level)
The primary objective of this study is to determine in women with node negative BC β€3cm in size, if PBI compared to WBI, both given once-a-day over 1 week following BCS, is non-inferior for LR and reduces adverse cosmesis. The primary outcomes are LR and patient-assessed cosmesis at 3 years post randomization.
Who can join: Review the eligibility criteria below.
Location: GenesisCare Darlinghurst β Darlinghurst, New South Wales
Age range: 50 Years to 120 Years
π§ͺ Interventions in This Study
- Whole Breast Irradiation (WBI) (RADIATION)
- Partial Breast Irradiation (PBI) (RADIATION)
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π All Participating Trial Locations (30 Sites)
Showing the first 25 of 30 sites.
- GenesisCare Darlinghurst β Darlinghurst, New South Wales
- GenesisCare Hurstville β Hurstville, New South Wales
- GenesisCare Mater Hospital β North Sydney, New South Wales
- GenesisCare Bundaberg β Bundaberg, Queensland
- GenesisCare Southport β Southport, Queensland
- GenesisCare Tugun β Tugun, Queensland
- GenesisCare Hervey Bay β Urraween, Queensland
- GenesisCare St Andrew's β Adelaide, South Australia
- GenesisCare Bedford Park β Bedford Park, South Australia
- GenesisCare Wembley β Wembley, Washington
- GenesisCare Fiona Stanley Hospital β Murdoch, Western Austrailia
- GenesisCare Hollywood β Nedlands, Western Australia
- Arthur J. E. Child Comprehensive Cancer Centre-Clinical Research Unit β Calgary, Alberta
- BCCA-Vancouver Island Cancer Centre β Victoria, British Columbia
- QEII HSC - Nova Scotia Cancer Centre β Halifax, Nova Scotia
- Royal Victoria Regional Health Centre β Barrie, Ontario
- Juravinski Cancer Centre β Hamilton, Ontario
- London Regional Cancer Centre β London, Ontario
- Stronach (Southlake) Regional Health Centre β Newmarket, Ontario
- Algoma District Cancer Program β Sault Ste. Marie, Ontario
- Princess Margaret Hospital β Toronto, Ontario
- Toronto-Sunnybrook Health Sciences Centre - Odette Cancer Centre β Toronto, Ontario
- Windsor Regional Cancer Centre β Windsor, Ontario
- CSSS Champlain - Charles LeMoyne β Greenfield Park, Quebec
- CHUM - Centre Hospitalier de L'UniversitΓ© de MontrΓ©al β Montreal, Quebec
π Contact the Study Coordinator
Phone: (905) 527-2299
Email: schamber@mcmaster.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
π° 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.
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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.