Clinically Significant Prostate Cancer

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

Condition / disease
Location
Status: Recruiting

Transperineal Versus Transrectal Cognitive Fusion Prostate Biopsy

This prospective randomized controlled trial aims to compare transperineal and transrectal cognitive fusion prostate biopsy techniques in patients with suspicious prostate lesions detected by multiparametric magnetic resonance imaging (mpMRI). Patients aged 50-75 years with PI-RADS 3-5 lesions on mpMRI and an indication for prostate biopsy will be randomly assigned in a 1:1 ratio to undergo either transperineal cognitive fusion prostate biopsy or transrectal cognitive fusion prostate biopsy. The primary objective of this study is to evaluate whether transperineal cognitive fusion biopsy is non-inferior to transrectal cognitive fusion biopsy in detecting clinically significant prostate cancer (csPCa). Secondary objectives include comparison of overall prostate cancer detection rates, detection of Gleason Grade Group ≥2 prostate cancer, biopsy-related infectious complications, other procedure-related complications, pain scores, and procedure duration. A total of 280 participants will be enrolled. Pathological evaluation will be performed after biopsy, and clinical outcomes and complications will be assessed during follow-up.

Participants needed: 280
Trial details
Age: 50-75Biological sex: MaleType: InterventionalSponsor: Ankara Etlik City HospitalUpdated: Jul 17, 2026Locations: 1
Eligibility criteria

Male patients aged 50-75 years. [+3]

Previous diagnosis of prostate cancer. [+4]

Status: Recruiting

Multimodal Imaging and Digital Pathology for Prostate Cancer Prediction

This is a multicenter observational study. A deep learning model integrated with multimodal imaging and digital pathology spatial registration is built based on preoperative multiparametric magnetic resonance imaging, transrectal ultrasound and postoperative digital pathological whole slide images. The study is designed to achieve accurate prediction of clinically significant prostate cancer and non-invasive risk stratification. Unnecessary prostate biopsy and overdiagnosis can be reduced to support the optimization of clinical diagnosis and treatment strategies.

Participants needed: 3,000
Trial details
Age: 40-90Biological sex: MaleType: ObservationalSponsor: Guangxi Medical UniversityUpdated: May 29, 2026Locations: 1Duration: 12 Years
Eligibility criteria

Subjects who are scheduled to undergo or have undergone prostate biopsy or radic... [+4]

Prior history of pelvic radiation therapy or radical prostatectomy. [+5]

Status: Recruiting

Plasma exoRNA-Based Liquid Biopsy to Diagnose Clinically Significant Prostate Cancer

The aim of the present study is to investigate a plasma exosome RNA signature to diagnose clinically significant prostate cancer.

Participants needed: 1,700
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: Xijing HospitalUpdated: Mar 25, 2026Locations: 10
Eligibility criteria

Blood prostate-specific antigen PSA>4ng/dl; [+2]

Previous diagnosis of prostate cancer through prostate biopsy; [+2]

Status: Recruiting

Study of PSMA PET/CT Imaging to Help Select Men With Low-Risk Prostate Cancer for Active Surveillance

This is a multicenter, prospective diagnostic accuracy study evaluating the Istanbul PSMA PET/CT Criteria (IPPC) for selecting patients with biopsy-confirmed low-risk prostate cancer (ISUP Grade 1) for active surveillance (AS). The study integrates delayed Ga-68 PSMA PET/CT imaging into the diagnostic pathway to refine patient stratification, minimize overtreatment and potentially reduce unnecessary biopsies and MRI, or exposing high-risk individuals to the danger of cancer progression if left untreated scans.

Participants needed: 201
Trial details
Age: 18+Biological sex: MaleType: ObservationalSponsor: Istanbul University - CerrahpasaUpdated: Sep 15, 2025Locations: 10Duration: 2 Years
Eligibility criteria

mpMRI performed within 3 months prior to enrollment [+8]

High-risk or unfavorable intermediate-risk PCa, or adverse histologies (neuroend... [+6]