Prostate Cancer Trial, Recruiting NCT07580196 Sponsor: University of Turin, Italy Condition: Prostate Cancer
Back to Prostate Cancer

Prostate Cancer Trial, Recruiting

NCT07580196
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:

  • Male patients aged 18 years or older
  • People with prostate cancer that has been confirmed by tissue testing and is considered high-risk, based on at least one of the following: a high aggressiveness score (ISUP Grade Group 4 or 5); scan findings suggesting the cancer may be spreading beyond the prostate on one side; or a PSA blood test result of 20 ng/mL or higher with the cancer mainly on one side
  • People whose cancer appears to be on one side of the prostate only, based on biopsy results and specialised scans (MRI and PSMA PET)
  • People whose specialised nuclear medicine scan (PSMA PET) does not show cancer spread to lymph nodes on the opposite side to the main cancer
  • People with no significant cancer activity detected on the opposite side of the prostate on PSMA PET scan
  • People with no confirmed cancer lesion on the opposite side of the prostate on MRI or biopsy
  • People with no high-risk or unusual cancer tissue found on the opposite side of the prostate
  • People with no sign of the cancer breaking through the prostate capsule or invading the seminal vesicles on the opposite side
  • People with a limited number of low-to-intermediate risk biopsy samples on the opposite side (up to two cores with unfavorable intermediate-risk disease, or up to four with favorable intermediate-risk disease) (confirm with trial site)
  • People with no more than two lymph nodes showing cancer activity on the same side as the main cancer on PSMA PET
  • People whose cancer appears confined to the prostate with no spread to distant sites or lymph nodes further away from the pelvis, confirmed by scans
  • People whose doctor estimates a life expectancy of more than 10 years
  • People who are scheduled for robot-assisted surgical removal of the prostate and are considered medically fit for surgery
  • People who have provided written consent to participate

Who may not be able to join:

  • People who have had any prostate cancer treatment before surgery, including hormone therapy, chemotherapy, radiation, or any procedure to destroy prostate tissue
  • People who have previously had active treatment for prostate cancer
  • People with high-grade cancer (ISUP Grade Group 4 or 5) on the opposite side of the prostate
  • People with certain amounts of intermediate-grade cancer on the opposite side of the prostate (more than four cores graded ISUP 2, or more than two cores graded ISUP 3)
  • People whose scans suggest the cancer has spread beyond the prostate on the opposite side
  • People whose scans show cancer has spread to lymph nodes or distant sites, except for up to two pelvic lymph nodes on the same side as the main cancer
  • People who have not had a sufficient prostate biopsy performed (a minimum of 10 cores is required, plus targeted samples when a target lesion is visible)
  • People with another currently active cancer
  • People who are unable to have MRI or PSMA PET scans for medical reasons
  • People who are unable to provide written informed consent
  • People aged under 18 years
  • People with a high anaesthetic risk score (ASA score greater than 3), indicating significant health concerns related to surgery
  • People with any medical reason that makes removal of pelvic lymph nodes unsafe
  • People with severe psychiatric illness
  • People with blood or clotting function that does not meet the required levels
  • People with an active infection
  • People with any serious medical, psychiatric, psychological, personal, or logistical condition that, in the investigator's judgement, could interfere with treatment, follow-up, or safety
  • People with a prior cancer that was treated with curative intent may only be considered if a local specialist multidisciplinary tumour board provides mandatory approval

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 15 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: Giancarlo Marra, MD, Principal Investigator

Phone: +39 011 633 6591

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
University of Turin, Italy
Registry
ClinicalTrials.gov
Start date
30 March 2026
Est. completion
1 December 2029

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

Biochemical Recurrence-Free Survival; PSA Persistence

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: 15 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