Prostate Cancer Trial, Recruiting
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 male and aged 18 years or older
- People who have prostate cancer with a calculated risk (using a tool called the Briganti nomogram) of cancer spreading to the lymph nodes of between 5% and 20%, and whose pre-surgery scan (called a PSMA PET/CT) shows no signs of cancer having spread
- People who are scheduled to have their prostate removed using a keyhole or robot-assisted surgical procedure
- People who have given written consent to take part
Who may not be able to join:
- People who have been rated as having very high anaesthetic risk (classified as ASA grade higher than 3) by their medical team
- People for whom lymph node removal surgery is not medically suitable
- People who have received hormone therapy before surgery (known as neoadjuvant hormone deprivation therapy)
- People who have not given consent, or who have withdrawn their consent to participate
- People whose pre-surgery PSMA PET/CT scan shows evidence that the cancer has already spread
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.
Contact this trial
Principal Investigator: Henk G van der Poel, Prof, The Netherlands Cancer Institute
Phone: 0205129111
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
Where this trial is recruiting
Primary endpoints
Persistent PSA rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 6 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.