Actively Recruiting

Age: 18Years +
MALE
NCT07334275

Detection of Minimal Residual Disease Post-prostatectomy

Led by Radboud University Medical Center · Updated on 2026-01-12

50

Participants Needed

1

Research Sites

119 weeks

Total Duration

On this page

Sponsors

R

Radboud University Medical Center

Lead Sponsor

C

Catharina Ziekenhuis Eindhoven

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Detection of Minimal Residual Disease Post-prostatectomy

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Male aged 18 years or older
  • High-risk localized prostate cancer with PSA >20 ng/mL, Gleason score 8-10 (ISUP grade 4/5), or stage iT3a by prostate MRI
  • High-risk locally advanced prostate cancer with any PSA level, any Gleason score/ISUP grade, stage iT3b-4 by prostate MRI or iN1 by PSMA PET/CT
  • Scheduled for robot-assisted radical prostatectomy
  • Willing to consent to tissue and liquid biobanking
Not Eligible

You will not qualify if you...

  • Relevant contra-indications limiting clinical follow-up or blood collection as judged by the physician

AI-Screening

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Trial Site Locations

Total: 1 location

1

Prosper Prostate Cancer Clinics

Nijmegen, Netherlands

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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