Prostate Cancer Trial, Recruiting NCT06451445 Sponsor: University Health Network, Toronto Condition: Prostate Cancer
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Prostate Cancer Trial, Recruiting

NCT06451445
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are over 50 years of age
  • People who are expected to live for at least 10 more years
  • People who have been diagnosed with prostate cancer through a tissue sample (biopsy), where the cancer is contained within the prostate and is at a clinical stage of T2c or lower
  • People whose PSA level (a blood marker for prostate cancer) is 15 ng/mL or below, or whose PSA density is below 0.15 ng/mL² if their PSA is above 15 ng/mL
  • People whose prostate cancer has a Gleason score of 3+4 or 4+3 (a measure of how the cancer cells look under a microscope)
  • People whose MRI scan shows no signs of the cancer spreading outside the prostate gland
  • People whose MRI scan shows no signs of the cancer reaching the seminal vesicles (small glands near the prostate)
  • People whose prostate gland can be clearly seen by the treating doctor using ultrasound during biopsy
  • People who have had a specific type of targeted prostate biopsy (guided by MRI findings), plus a wider systematic biopsy of 10–14 samples, confirming a Gleason score of 7 only in the area identified on MRI, with no Gleason 7 or higher cancer found outside that area
  • People who have a lesion (abnormal area) visible on MRI that can be reached by the Irreversible Electroporation (IRE) treatment used in this trial (confirm with trial site for details about nearby biopsy findings)
  • People who are willing and able to sign a consent form agreeing to take part
  • People who are able and willing to attend all required follow-up appointments

Who may not be able to join:

  • People who have a known allergy or sensitivity to pancuronium bromide, atracurium, or cisatracurium (medicines used to relax muscles during procedures)
  • People who are not suitable for general anaesthesia or cannot receive the muscle-relaxing medicines used in this trial
  • People who currently have a urinary tract infection (UTI)
  • People who have a history of bladder neck contracture (scarring that narrows the bladder opening)
  • People who wish to have children in the future
  • People who have had inflammatory bowel disease within the past 3 years
  • People who have another serious or debilitating illness at the time of the trial
  • People who have received active treatment for any cancer (other than prostate cancer or non-melanoma skin cancer) within the past 3 years — people considered to be in remission for at least 3 years by their cancer care provider may be eligible (confirm with trial site)
  • People who have any active implanted electronic device, such as a pacemaker
  • People who are unable or unwilling to use a urinary catheter (a tube used to drain the bladder)
  • People who have previously received any treatment for prostate cancer, including biological therapy, chemotherapy, hormone therapy (within three months of the procedure), radiation therapy, or surgery for prostate cancer
  • People who have previously had surgery for urethral stricture (narrowing of the urine tube), a urethral stent, or any implants placed in the prostate
  • People who have had major surgery on the rectum in the past (other than for haemorrhoids)
  • People who are not suitable for a pelvic MRI scan — for example, due to severe claustrophobia, a permanent pacemaker, certain metal implants that would interfere with imaging, or an allergy or other reason they cannot receive gadolinium (a contrast dye used to enhance MRI images)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
16 May 2024
Est. completion
1 May 2028

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Rate of negative in-field biopsy at 12 months; Incidence of adverse events by type and CTCAE v5.0 severity through 12 months

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov