Prostate Cancer Trial, Recruiting NCT06052683 Sponsor: CHU de Quebec-Universite Laval Condition: Prostate Cancer
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Prostate Cancer Trial, Recruiting

NCT06052683
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 confirmed by biopsy to have prostate adenocarcinoma (a specific type of prostate cancer) diagnosed within the last 8 months — including people on active surveillance whose cancer has shown signs of progression and who have had a recent biopsy within 8 months.
  • People whose cancer is classified as either "low-risk" or "favourable intermediate-risk" based on specific tumour stage, Gleason score (a measure of cancer aggressiveness), and PSA blood test levels (confirm with trial site for exact classification).
  • People aged 18 or older.
  • People who are generally active and able to care for themselves, with little to no limitation in daily activities (this is measured using a standard medical scale called ECOG performance status 0–1).
  • People who a treating doctor has determined are medically suitable for a type of internal radiation treatment called LDR brachytherapy.
  • People whose prostate gland measures 60 cc or smaller, as measured by ultrasound, CT, or MRI within the last 6 months.
  • People with an International Prostate Symptom Score (a standard questionnaire about urinary symptoms) of 20 or below — medication called alpha blockers is permitted.
  • People who have not used a type of medication called alpha reductase inhibitors within two weeks before being enrolled in the trial.
  • People who have not received hormonal therapy for their prostate cancer.
  • People who are willing and able to complete a set of study questionnaires about prostate cancer outcomes, urinary symptoms, and sexual health.
  • People who have signed the study's informed consent form before joining.

Who may not be able to join:

  • People whose cancer has spread to other parts of the body or to lymph nodes, based on clinical or imaging findings.
  • People whose cancer has reached a clinical stage higher than T2a (a measure of how far the tumour has grown within or beyond the prostate).
  • People with a Gleason score of 4+3 or higher (indicating a more aggressive cancer pattern).
  • People with a history of other cancers, unless it was a non-melanoma skin cancer that was adequately treated, or another solid cancer that was fully treated with no signs of return for at least 3 years.
  • People who have previously had radical (complete) surgery to remove the prostate, or a procedure called TURP (a surgical procedure to remove part of the prostate).
  • People who have previously had radiation treatment to the pelvis, or any prior radiation that would overlap with the area to be treated in this trial.
  • People who have received chemotherapy for prostate cancer, or any chemotherapy within the last 3 years.
  • People who have previously had cryosurgery (a freezing treatment) on the prostate.
  • People who have a current or past bleeding disorder that would make placing small markers in the prostate or performing the brachytherapy procedure unsafe.
  • People who have received androgen deprivation therapy (a hormone-reducing treatment) within 6 months before registering for the trial.
  • People who have bilateral hip prostheses (artificial replacements in both hips).
  • People with serious active health conditions, uncontrolled infections, significant psychiatric illness, severe laboratory abnormalities, or other medical conditions — such as active inflammatory bowel disease or significant urinary symptoms — that the trial investigator determines would prevent safe participation.

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 28 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: Isabelle Thibault, MD, FRCPC, CHU de Québec-Université Laval

Phone: 418-525-4444

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
CHU de Quebec-Universite Laval
Registry
ClinicalTrials.gov
Start date
30 September 2019
Est. completion
30 September 2028

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Adverse Event Evaluation according to the CTCAE version 4 to assess non-inferiority of SBRT compared to LDRB.

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: 28 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