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Clinical Trials/NCT06016595
NCT06016595
Completed
Not Applicable

Retrospective Data Analysis in Chronic Prostatitis/Chronic Pelvic Pain Syndrome Patients: Evaluation of the Relationship Between Presence of Microorganism and Severity of Symptom

Hisar Intercontinental Hospital1 site in 1 country112 target enrollmentJanuary 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Prostatitis With Chronic Pelvic Pain Syndrome
Sponsor
Hisar Intercontinental Hospital
Enrollment
112
Locations
1
Primary Endpoint
Correlation between androflor pcr positive patients and uopint and nih-cpsi
Status
Completed
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 1, 2020
End Date
May 10, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Basri Cakiroglu

Ass. Prof.

Hisar Intercontinental Hospital

Eligibility Criteria

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

Outcomes

Primary Outcomes

Correlation between androflor pcr positive patients and uopint and nih-cpsi

Time Frame: 2 years

Those with positive and negative Androflor PCR test will be evaluated. testicular torsion

Study Sites (1)

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