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Prospective Prostate Cancer and Patient-reported Outcomes Registry

Recruitingn/aAges 18 Years - anyMaleUniversitaire Ziekenhuizen KU Leuven
NCT04694924 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This study aims to evaluate the use of a digital solution, integrated into the electronic health record, for prospective and structured reporting of clinical and patient-reported outcomes for patients diagnosed with localized or locally advanced prostate cancer.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Pathology confirmed diagnosis of localized or locally advanced prostate cancer * Being able to speak, read and understand Dutch, French, or English * Each patient (or their legally acceptable representative) must sign an informed consent form (ICF) indicating that he understands the purpose of, and is willing to participate in the study. Exclusion Criteria: * Patients with prior treatment for prostate malignancies will be excluded. * Dementia, mental alteration, or psychiatric pathology that can compromise informed consent from the patient and/ or adherence to the protocol and the monitoring of the trial * Patients who cannot submit themselves to following the protocol for psychological reasons, social, family, or geographical. * Persons deprived of liberty or under guardianship
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What it tests

  • standard of care
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Where

4 sites
AZ Sint-Blasius
Dendermonde, Belgium
University Hospitals Leuven
Leuven, Belgium
AZ Sint-Jan Brugge
Bruges, Belgium
AZ Groeninge Kortrijk
Kortrijk, Belgium
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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