NCT07422597Recruiting
Prostate Risk Or Radiology Assessment Non-inferiority Design, Upfront MRI or Risk Calculator in Men With Suspected Prostate Cancer
PRORAND - Prostate Risk or Radiology Assessment Non-inferiority Design, a Comparison of Upfront MRI vs Risk Calculator in Men With Suspected Prostate Cancer
Source: ClinicalTrials.gov · Last updated 21 Oct 2026
Brief summary (registry, in English)
Thousands of men take a PSA test to investigate whether they have prostate cancer every year. For the vast majority, the test is normal and further investigations are not necessary. In others, the test is sufficiently elevated that men are referred for further investigations. Most men with an elevated PSA are offered an MRI examination of the prostate gland, and for some, a tissue sample of the prostate is also recommended if the suspicion of cancer is high enough. Although this comprehensive investigation reveals most clinically significant , or dangerous cases of cancer, many indolent, or "harmless" cancer cases are also detected, which would not have caused the man any harm during his lifetime (approximately 20% of all prostate cancer diagnoses diagnosed in current clinical practive). Cancer treatment is not recommended for such cases, but for many men, the diagnosis and subsequent follow-up can cause him and his family anxity and concern. In addition, prostate biopsies are unpleasant for the patient and the investigation process is resource-intensive for both the man and the health care service. Risk stratification uses machine learning methods to better identify the men who require further investigations with MRI and tissue samples. In this project, the investigators investigate whether the best risk stratification tools are non-inferior in detecting clinically significant prostate cancer compared to current practice, and whether they lead to fewer tissue samples, MRI scans, less health anxiety, and better cost-effectiveness.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 1016 (estimated)
- First submitted
- 30 Dec 2025
- Start date
- 1 Mar 2026
- Primary completion date
- 31 Dec 2027
- Lead sponsor
- Norwegian University of Science and Technology
- Diseases
- Prostate cancer
- NCT number
- NCT07422597
What you commit to
- Study type: Interventional
- Planned participants: 1016
- From 1 Mar 2026 to the primary completion date, 31 Dec 2027
- 3 sites 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.
Prior treatment
- Prior diagnosis of prostate cancer
Lab values
- Medications known to affect serum PSA levels
Other
- cT3 and/or cT4 (on DRE)
- PSA \>20 ng/ml
- Contraindications to MRI or to prostate biopsy
Who the study is looking for
- more than 10 years remaining life expectancy
- Suspected localized prostate cancer
- Suspicious DRE (cT2)
- PSA 3-20 ng/ml
Age in the registry: 50 years to 75 years · Sex: Male · Accepts healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Sykehuset Levanger Coordinator of this site? Confirm its status | Levanger | Norway | Not yet recruiting |
| Orkdal sjukehus Coordinator of this site? Confirm its status | Orkanger | Norway | Recruiting |
| St Olavs Hospital Coordinator of this site? Confirm its status | Trondheim | Norway | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.