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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05179707
Other study ID # CSZ01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2022
Est. completion date October 1, 2023

Study information

Verified date January 2022
Source Qilu Hospital of Shandong University
Contact Shouzhen Chen, Dr.
Phone 18560089085
Email chensz@mail.sdu.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Before prostate puncture, the patient's serum was collected for PHI detection, and multi-parameter MRI was performed to obtain the PI-RADS score. The sensitivity and specificity of PHI combined with PI-RADS score in the diagnosis of clinically significant prostate cancer were explored.


Description:

This study is a multi-center prospective study. Patients who meet the indications for prostate puncture and whose PSA is in the gray area (4.0~10.0 ng/mL) undergo standard prostate biopsy. The patient's serum was collected for PHI detection before puncture, and multi-parameter MRI was performed before puncture. To explore the sensitivity and specificity of PHI combined with PI-RADS score in the diagnosis of clinically meaningful prostate cancer. Assess the benefit of combining PHI and mpMRI before biopsy compared with phi or mpMRI alone. Formulate clinical recommendations for PHI and mpMRI.


Recruitment information / eligibility

Status Recruiting
Enrollment 936
Est. completion date October 1, 2023
Est. primary completion date October 1, 2023
Accepts healthy volunteers
Gender Male
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria: - Patients with suspected prostate cancer - Patients can perform standardized prostate biopsy Exclusion Criteria: - Have a history of prostate cancer - Use of drugs that affect PSA before blood sampling

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Qilu hospital Jinan Shandong

Sponsors (2)

Lead Sponsor Collaborator
Qilu Hospital of Shandong University Zibo Central Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prostate Health Index PHI is a simple, FDA-approved blood test that helps determine the probability of detecting prostate cancer with a biopsy. This test uses an algorithm to assess total PSA, free PSA, and p2PSA, 1 year
Primary PI-RADS score In PI-RADS, based on the comprehensive manifestations of prostate T2WI, DWI and DCE, a scoring method is given for the possibility of clinically significant prostate cancer. Specifically: 1 point: very low, extremely unlikely to exist; 2 points: low, impossible to exist; 3 points: moderate, suspicious existence; 4 points: high, may exist; 5 points: very high, extremely likely to exist. 1 year
Primary Prostate biospy pathology The pathological results of prostate puncture are used as the gold standard for the diagnosis of prostate cancer, indicating whether the patient is really suffering from prostate cancer 1 year
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