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Risk Factors for Chronic Prostatitis Patients in Northwest China

Recruiting
Conditions
Chronic Prostatitis With Chronic Pelvic Pain Syndrome
Interventions
Behavioral: lifestyle
Behavioral: sexual habits
Drug: medication
Registration Number
NCT06385977
Lead Sponsor
Shaanxi Provincial People's Hospital
Brief Summary

The goal of this observational study is to learn about the risk factors of lifestyle, medication and sexual habits in adult chronic prostatitis / chronic pelvic pain syndrome patients. The main questions it aims to answer are:

* Is lifestyle, medication, and sexual habits related to chronic prostatitis / chronic pelvic pain syndrome

* Is there any medication available to protect men from chronic prostatitis / chronic pelvic pain syndrome.

Participants will:

* Independently receive a survey questionnaire on lifestyle, medication, and sexual habits.

* Symptomatic individuals will undergo additional prostate fluid examination for diagnosis.

Researchers will compare healthy adult males to see if there are differences on lifestyle, medication and sexual habits between the two groups.

Detailed Description

All participants were asked to fill out a questionnaire which was modified based on Zhang Ran's research. The questionnaire contained the following parts: patient's general situation, dietary habits, disease status, medication, lifestyle, sexual habits and NIH-CPSI index (National Institutes of Health Chronic Prostatitis Symptom Index). Furthermore, the patients underwent digital rectal examination, expressed prostatic secretion microscopy and microbial culture, urinalysis, urine microbial culture and transrectal ultrasonography.

Recruitment & Eligibility

Status
RECRUITING
Sex
Male
Target Recruitment
400
Inclusion Criteria
  • Discomfort or pain in the pelvic region or perineum;
  • Symptoms lasting for at least 3 months;
  • NIH-CPSI pain score of ≥ 4;
  • Controls are volunteers who do not present any prostatitis-related symptoms.
Exclusion Criteria
  • Prostate cancer;
  • Benign prostatic hyperplasia with a post-void residual urine volume of >50 ml;
  • Acute urinary tract infection.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
case groupsexual habitsparticipates diagnosed with Chronic prostatitis/chronic pelvic pain syndrome
case groupmedicationparticipates diagnosed with Chronic prostatitis/chronic pelvic pain syndrome
control grouplifestyleparticipates without Chronic prostatitis/chronic pelvic pain syndrome
control groupsexual habitsparticipates without Chronic prostatitis/chronic pelvic pain syndrome
case grouplifestyleparticipates diagnosed with Chronic prostatitis/chronic pelvic pain syndrome
control groupmedicationparticipates without Chronic prostatitis/chronic pelvic pain syndrome
Primary Outcome Measures
NameTimeMethod
Odds Ratiobaseline

The ratio of exposed to unexposed individuals in the case group divided by the ratio of exposed to unexposed individuals in the control group

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Shaanxi Provincial People's Hospital

🇨🇳

Xi'an, Shaanxi, China

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