Risk Factors for Chronic Prostatitis/Chronic Pelvic Pain Syndrome Patients in Northwest China
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 400
- Locations
- 1
- Primary Endpoint
- Odds Ratio
Study Overview
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.
Study Design
- Study Type
- Observational
- Observational Model
- Case Control
- Time Perspective
- Retrospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- Male
- Accepts Healthy Volunteers
- Yes
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.
Arms & Interventions
case group
participates diagnosed with Chronic prostatitis/chronic pelvic pain syndrome
Intervention: lifestyle (Behavioral)
case group
participates diagnosed with Chronic prostatitis/chronic pelvic pain syndrome
Intervention: sexual habits (Behavioral)
case group
participates diagnosed with Chronic prostatitis/chronic pelvic pain syndrome
Intervention: medication (Drug)
control group
participates without Chronic prostatitis/chronic pelvic pain syndrome
Intervention: lifestyle (Behavioral)
control group
participates without Chronic prostatitis/chronic pelvic pain syndrome
Intervention: sexual habits (Behavioral)
control group
participates without Chronic prostatitis/chronic pelvic pain syndrome
Intervention: medication (Drug)
Outcomes
Primary Outcomes
Odds Ratio
Time Frame: baseline
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 Outcomes
No secondary outcomes reported