A Diagnostic Prediction Model for Prostate Cancer in Patients With PI-RADS Score 3
NCT ID: NCT06507462
Last Updated: 2025-02-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
460 participants
OBSERVATIONAL
2021-01-01
2024-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
* Construct a diagnostic model of patients with PI-RADS of score.
* Internal and external validation of the model.
* Decision curve analysis. The data of participants was collected retrospectively.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
PSMA PET/MRI-Guided Prostate Biopsy for PI-RADS ≤3 and Prior Negative Biopsy
NCT06923657
Comparison of 5.0T and 3.0T Biparametric Magnetic Resonance Imaging in the Diagnosis of Prostate Cancer
NCT06612047
Pathological Positivity Rate in Prostate Cancer Patients with PI-RADS 4 and First Negative Biopsy
NCT06677775
Radical Prostatectomy Without Prostate Biopsy Following PSMA PET/CT Based on Diagnostic Model
NCT05587192
The Addictive Diagnostic Value of Apparent Diffusion Coefficients to bpMRI in the Diagnosis of Prostate Cancer
NCT06737588
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients with clinical suspicion of prostate cancer and have PI-RADS score of 3
Patients with clinical suspicion of prostate cancer (see inclusion criteria) and have PI-RADS score (results of mpMRI) of 3.
prostate biopsy
All patients were required to underwent transperineal prostate biopsy and have corresponding pathological diagnosis results.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
prostate biopsy
All patients were required to underwent transperineal prostate biopsy and have corresponding pathological diagnosis results.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. All patients have undergone mpMRI and have complete imaging data;
3. The PI-RADS score of patients was 3;
4. Prostate biopsy was performed and has clear pathological results.
Exclusion Criteria
2. Repeated prostate biopsy;
3. The patient's clinical, imaging, or pathological data are incomplete.
18 Years
MALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Anhui Provincial Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
XiaoJun
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jun Xiao, Pro.
Role: PRINCIPAL_INVESTIGATOR
The First Affiliated Hospital of USTC
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Urology, The First Affiliated Hospital of Bengbu Medical University
Bengbu, Anhui, China
Department of Urology, The First Affiliated Hospital of USTC
Hefei, Anhui, China
Department of Urology, The First Affiliated Hospital of Wannan Medical College
Wuhu, Anhui, China
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2024-ky312
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.