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NCT07334275Recruiting

Detection of Minimal Residual Disease Post-prostatectomy

Pilot Study for the Detection of Minimal Residual Disease Post-prostatectomy and Early Disease Recurrence in Circulating Tumor DNA to Guide Future Adjuvant Therapy in High-risk Prostate Cancer Patients (MiRaDE)

Source: ClinicalTrials.gov · Last updated 12 Jan 2026

Brief summary (registry, in English)

The clinical objective for this pilot study is to determine whether minimal residual disease (MRD) detection in high-risk prostate cancer, utilizing a custom-made prostate-specific circulating tumor DNA (ctDNA) panel, may lead to more optimal prediction of disease recurrence following radical prostatectomy.

Status (registry)
Recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
31 Dec 2025
Start date
16 Sept 2025
Primary completion date
Jul 2027
Lead sponsor
Radboud University Medical Center
NCT number
NCT07334275

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 16 Sept 2025 to the primary completion date, Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Relevant contra-indications that may limit clinical follow-up or blood collection, as assessed by the including physician.

Who the study is looking for

  • Male aged 18 years or older;
  • High-risk prostate cancer, defined as:
    • High-risk localized prostate cancer, with PSA level \>20 ng/mL, Gleason score 8-10 (ISUP grade 4/5) at prostate biopsies, or iT3a (based on multi-parametric MRI of the prostate); or
    • High-risk locally advanced prostate cancer, having any PSA level, any Gleason score/ISUP grade, iT3b-4 (based on multi-parametric MRI of the prostate) or iN1 (based on PSMA PET/CT imaging);
  • Scheduled for robot-assisted radical prostatectomy;
  • Willingness to consent to both patient information sheets regarding tissue and liquid biobanking.

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Prosper Prostate Cancer Clinics
Coordinator of this site? Confirm its status
NijmegenNetherlandsRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.