Prostate Cancer Trial, Recruiting NCT04004312 Sponsor: Fabio Cury Condition: Prostate Cancer
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Prostate Cancer Trial, Recruiting

NCT04004312
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 have been diagnosed with prostate adenocarcinoma (a specific type of prostate cancer), confirmed by a tissue sample
  • People with an early-stage prostate cancer (T1–T2b based on a specific staging system) with a cancer aggressiveness score (Gleason score) of 6 or 7 (3+4), or a Gleason score of 7 (4+3) with a recent PSA blood test result below 10 ng/mL
  • People with a recent PSA blood test result below 15 ng/mL — or, for Gleason 7 (4+3), below 10 ng/mL — taken within the last 30 days (with specific timing rules if certain prostate medications were recently stopped — confirm with trial site)
  • People with a urinary symptom score below 16 on a standard questionnaire (International Prostate Symptom Score)
  • People whose prostate gland measures less than 80cc in volume
  • People with a good general health and activity level, assessed within the 60 days before registration (rated 0–1 on a standard scale used in clinical trials)
  • People aged 18 or older
  • People who are able to give their informed consent before the study begins

Who may not be able to join:

  • People who have chosen another treatment for their prostate cancer, such as surgery or active surveillance (watchful waiting)
  • People with a history of another invasive cancer (other than certain minor skin cancers) or blood/lymph cancers, unless there has been no sign of disease for at least 5 years — people with certain non-invasive (in situ) cancers may still be considered eligible, except those with any history of bladder cancer (confirm with trial site)
  • People with evidence that cancer has spread to distant parts of the body
  • People whose cancer has spread to nearby lymph nodes
  • People who have previously had radical prostate surgery (prostatectomy), cryosurgery, or high-intensity focused ultrasound (HIFU) for prostate cancer
  • People who have previously had pelvic radiation therapy, prostate brachytherapy (internal radiation), or surgical removal of both testicles
  • People who have previously had hormone therapy for prostate cancer, including certain injections, tablets, or surgical castration
  • People who have taken the medication finasteride within the 30 days before registration
  • People who have taken the medication dutasteride within the 90 days before registration
  • People who have had or are currently receiving chemotherapy for prostate cancer
  • People with serious active health conditions, including any of the following:
    • Unstable chest pain (angina) or heart failure that required hospitalisation in the past 6 months
    • A major heart attack in the past 6 months
    • An active bacterial or fungal infection currently being treated with intravenous antibiotics
    • A severe breathing condition or lung illness currently requiring hospitalisation or that would prevent participation in the study
    • Significant liver disease causing visible jaundice or serious problems with blood clotting (note: people taking blood-thinning medications such as Coumadin are not excluded)
    • A diagnosis of AIDS as defined by current public health guidelines (note: HIV testing is not required to join — confirm with trial site)

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 16 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.

Contact this trial

Principal Investigator: Fabio Cury, MD, McGill University Health Centre- Cedars Cancer Centre

Phone: 514-934-1934

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Fabio Cury
Registry
ClinicalTrials.gov
Start date
7 November 2018
Est. completion
31 January 2027

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Small bowel or rectal irritation,; Bladder complications

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: 16 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