About this trial
The purpose of this clinical trial is to evaluate the efficacy of Jing Si Herbal Tea as an adjuvant treatment for patients diagnosed with Chronic Pelvic Pain Syndrome (CPPS). The study aims to determine whether adding Jing Si Herbal Tea to standard care can improve clinical symptoms and quality of life in these patients.
Eligibility criteria
Qualifiers
Male patients.
Diagnosed with Chronic Pelvic Pain Syndrome (CPPS) at the investigational site.
Currently receiving continuous follow-up and medical treatment.
Disqualifiers
Female patients (Excluded because the standard treatment, alpha-blockers, is not approved or reimbursed by the National Health Insurance for this indication in women in Taiwan).
Duration of symptoms less than 3 months.
History of recurrent urinary tract infections.
Diagnosed with malignancy.
Trial design
Treatments tested in this trial
- Jing Si Herbal Tea
- Placebo