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Needle Localization During Prostate Brachytherapy Using Power Doppler Ultrasound

W

Western University, Canada

Status

Enrolling

Conditions

Prostate Cancer

Treatments

Device: Prostate Brachytherapy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study involves patients who are scheduled for standard care brachytherapy of focal tumours within the prostate, which is normally performed under standard 2-dimensional (2D) ultrasound guidance. The purpose of this study is the acquire power Doppler ultrasound while using a simple oscillator in physical contact with the end of a brachytherapy needle. The vibrations along the needle should be visible in the power Doppler ultrasound, helping to visualize the needle position within the anatomy.

Enrollment

20 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Patient
Other group
Description:
Patient undergoing standard care prostate high dose rate brachytherapy.
Treatment:
Device: Prostate Brachytherapy

Trial contacts and locations

1

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Central trial contact

Aaron Fenster

Data sourced from clinicaltrials.gov

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