๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-12-10

Focal Versus Whole Gland High Dose-Rate Brachytherapy (HDR-BT) Boost to External Beam Radiotherapy in Localized Prostate Cancer: A Phase 2 Randomized Trial (NCT07300566)

FOcal Versus Whole Gland High Dose-Rate Brachytherapy (HDR-BT) Boost With ExternAl Beam Radiotherapy in LocalizeD Prostate Cancer: A Phase 2 Randomized Trial [FORWARD]

๐ŸŸก Not Yet Recruiting Phase2 ๐Ÿ“‹ Clinical Research Protocol Sponsor: Joelle Helou

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

This project aims to compare the changes in the urinary quality of life (QoL) following focal high dose-rate brachytherapy (HDR-BT) boost to stereotactic ablative radiotherapy (SABR), compared to standard whole gland HDR-BT boost, in the treatment of men diagnosed with intermediate- and high-risk prostate cancer, with have an identifiable DIL on mpMRI.

Who can join: Review the eligibility criteria below.

Location: London Health Sciences Centre, Verspeeten Family Cancer Centre โ€” London, Ontario

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • Standard Arm: Whole Gland High Dose Rate Brachytherapy Boost (RADIATION)
  • Experimental Arm: Focal High Dose Rate Brachytherapy Boost (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 (1 Sites)

  • London Health Sciences Centre, Verspeeten Family Cancer Centre โ€” London, Ontario

๐Ÿ“ž Contact the Study Coordinator

Phone: (519) 685-8650

Email: Joelle.Helou@lhsc.on.ca

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 Prostate 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†—