Chronic Prostatitis/Chronic Pelvic Pain Syndrome Patients

Completed

• Conditions: Chronic Prostatitis With Chronic Pelvic Pain Syndrome
• Interventions: Diagnostic Test: Chronic prostatitis/chronic pelvic pain syndrome

• Registration Number: NCT06016595
• Lead Sponsor: Hisar Intercontinental Hospital

Brief Summary

Chronic prostatitis/chronic pelvic pain syndrome (CPPS) is a common health problem among men and can cause severe quality of life. The pathophysiology of CPPS is still poorly understood and effective treatments are a challenging issue. This study aims to investigate the possible relationship between the presence of microorganisms in the prostatic fluid and symptom severity by presenting a retrospective analysis based on data from CPPS patients.

Detailed Description

This study is based on data from 112 CPPS patients aged 20-60 years. Various variables such as demographic information of the patients, International Prostate Symptom Score (I-PSS), which evaluates CPPS symptoms, inflammatory and non-inflammatory symptoms of CPPS, baseline scores of the International Index of Erectile Function (IIEF), which evaluates erectile function, and the presence of microorganisms in the prostate fluid were analyzed retrospectively.

Study Timeline

• Study Start: 2020-01-01
• Primary Completion: 2022-12-31
• Study Completion: 2023-05-10
• Status Verified: 2023-08
• Study First Submitted: 2023-08-16
• Study First Submitted QC: 2023-08-28
• Last Update Submitted: 2023-08-28
• Study First Posted: 2023-08-29
• Last Update Posted: 2023-08-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 112

Inclusion Criteria

• Patients who were diagnosed with chronic prostatitis/chronic pelvic pain syndrome and whose prostate fluid was taken with prostate massage and androflor testis were studied were included.

Exclusion Criteria

• acute and/or chronic bacterial prostatitis, active history of genitourinary cancer, history of recent prostate surgery the diagnosis of neurological diseases affecting the bladder was determined

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
singel	Chronic prostatitis/chronic pelvic pain syndrome	-

Primary Outcome Measures

Name	Time	Method
Correlation between androflor pcr positive patients and uopint and nih-cpsi	2 years	Those with positive and negative Androflor PCR test will be evaluated. testicular torsion

Trial Locations

Locations (1)

Hisar Intercontinental Hospital; 🇹🇷 Istanbul, Turkey