Prostate Cancer Trial, Recruiting NCT06215508 Sponsor: University of Chicago Condition: Prostate Cancer
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Prostate Cancer Trial, Recruiting

NCT06215508
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 a specific type of prostate cancer (adenocarcinoma of the prostate) confirmed by a tissue or cell sample, without certain rare cell types present.
  • People whose cancer has spread (metastasised) to at least one other part of the body, as seen on a bone scan, CT scan, MRI, or certain specialised imaging scans.
  • People aged 65 years or older.
  • People who are about to start an intensified hormone-blocking treatment plan that combines two specific types of hormone therapy (ADT and ARSI).
  • People who are able to understand the study and are willing to sign a written consent form.

Who may not be able to join:

  • People who have previously received hormone-blocking therapy (ADT or ARSI) within 12 months of their diagnosis, unless that treatment was started within 12 weeks of enrolling in the trial.
  • People who had surgical removal of the testicles more than 12 weeks before their metastatic cancer diagnosis.
  • People who have previously received chemotherapy for metastatic prostate cancer.
  • People who have another illness that is not well controlled or stable at the time of enrolment, such as poorly managed diabetes or high blood pressure (confirm with trial site).
  • People who have a specific rare type of prostate cancer called small-cell carcinoma, or who have cancer that has spread to the brain.
  • People who are not able to read and write in English or Spanish.
  • People who are pregnant or are not biological males, as this trial is specifically for prostate cancer in biological males.
  • People who have an implanted cardiac (heart) device, such as a pacemaker.
  • People who have a limb difference or condition that would prevent them from wearing a smartwatch.

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 13 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

Phone: 8557028222

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
Registry
ClinicalTrials.gov
Start date
1 April 2026
Est. completion
1 April 2031

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Cancer and Aging Research Group (CARG) scores

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: 13 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