Active Surveillance for Prostate Cancer

2

Review clinical trials related to Active Surveillance for Prostate Cancer. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Stockholm3 Test Validation in Men on Active Surveillance in Switzerland (CHAS3 Trial)

The CHAS3 trial studies whether the Stockholm3 blood test can reliably detect if prostate cancer becomes more aggressive in men who are being carefully monitored instead of treated right away (active surveillance). The goal is to see if this test can help doctors safely follow patients with fewer invasive procedures, such as repeated biopsies.

Participants needed: 350
Trial details
Biological sex: MaleType: ObservationalSponsor: Insel Gruppe AG, University Hospital BernUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Adult Men ≥ 18 y. o. [+3]

- Prior prostate cancer treatment (surgery, radiation, chemotherapy, hormonal th... [+3]

Status: Not yet recruiting

Micro-Ultrasound for Detecting Clinically Significant Prostate Cancer in Active Surveillance

Active surveillance is a common approach for men with low-risk or favorable intermediate-risk prostate cancer, aimed at avoiding or delaying treatment while closely monitoring the disease. Multiparametric MRI (mpMRI) is widely used to guide diagnosis and follow-up, but it can miss clinically significant prostate cancer and may be limited by access, cost, and variability in interpretation. Micro-ultrasound is a high-resolution ultrasound technique that may improve real-time detection of suspicious prostate lesions using a standardized scoring system (PRI-MUS). The purpose of this study is to evaluate the diagnostic performance of micro-ultrasound for detecting clinically significant prostate cancer in men with negative or stable mpMRI findings, either at initial diagnosis or during active surveillance follow-up. Participants will undergo micro-ultrasound assessment of the prostate. Areas considered suspicious on micro-ultrasound may be targeted for biopsy, followed by systematic prostate sampling. Biopsy results will be used as the reference standard to determine whether clinically significant prostate cancer is present. The study will assess measures such as sensitivity, specificity, and predictive values of micro-ultrasound, as well as procedure-related complications.

Participants needed: 90
Trial details
Age: 45-75Biological sex: MaleType: InterventionalSponsor: McGill University Health Centre/Research Institute of the McGill University Health CentreUpdated: Feb 4, 2026Locations: 1
Eligibility criteria

Male participants aged 45 to 75 years [+8]

Prior definitive treatment for prostate cancer (e.g., radical prostatectomy, rad... [+4]