Using power Doppler ultrasound to improve needle localization during prostate brachytherapy
Official title: Needle Localization During Prostate Brachytherapy Using Power Doppler Ultrasound
Run by Western University, Canada · NCT03861507 · Data updated 2026-11-12
This study is testing whether using power Doppler ultrasound can help doctors place needles more accurately during prostate cancer treatment.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Men only |
| Enrollment | 20 (estimated) |
| Sponsor | Western University, Canada Academic / other |
| Locations | 1 site (London, Ontario) |
| Status | Recruiting |
| Started | March 4, 2020 |
| Main results expected | August 2025 |
| Study ends | December 2025 |
| Registry record updated | March 28, 2025 |
| Trial ID | NCT03861507 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are males aged 18 years or older with pathologically confirmed prostate cancer who are suitable for high-dose-rate brachytherapy.
✕Probably not a fit
Patients who have previously received radiotherapy to the prostate may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study focuses on patients scheduled for standard brachytherapy treatment for prostate cancer. It aims to enhance the visualization of needle placement by utilizing power Doppler ultrasound in conjunction with a simple oscillator attached to the brachytherapy needle. The vibrations transmitted through the needle are expected to be captured by the ultrasound, providing better guidance during the procedure. This innovative approach seeks to improve the accuracy of needle localization compared to traditional 2D ultrasound methods.
Why it matters
Potential benefit: If successful, this method could lead to more precise brachytherapy treatments, potentially improving patient outcomes and reducing complications.
How similar studies have gone: While this approach is innovative, similar studies using advanced imaging techniques in brachytherapy have shown promise in improving treatment accuracy.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male, aged 18 years or older * Willing to provide written consent * Pathologically confirmed prostate cancer on previous biopsy * Suitable for and consenting to high-dose-rate brachytherapy for treatment as standard of care. Exclusion Criteria: * • Previous radiotherapy to the prostate
Where it's running
-
Victoria Hospital
London, Ontario, Canada Recruiting
Study contacts
- Study coordinator: Aaron Fenster
- Email: afenster@uwo.ca
- Phone: 5199315777
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.