Pentosan Polysulfate Treatment's Effectiveness
- Conditions
- Chronic Interstitial Cystitis
- Interventions
- Other: Pentosan Polysulphate
- Registration Number
- NCT05744908
- Lead Sponsor
- Hisar Intercontinental Hospital
- Brief Summary
To examine the relationship between symptoms and quality of life before and after oral pentosan polysulfate (PPS) treatment in cases diagnosed with interstitial cystitis/painful bladder syndrome (IC/BPS).
- Detailed Description
Demographic characteristics, medical history, clinical conditions, and laboratory and cystoscopic data of patients who applied to our clinic between January 2018 and December 2021 and were diagnosed with IC/BPS were retrospectively analyzed. Adult male and female patients with IC/BPS who received 300 mg/day PPS at least six months ago with complaints of pain, urge, frequency, and nocturia not associated with urinary tract infection were included in the study. In addition, pre- and post-treatment symptoms, ICSI scores, quality of life (scored between 1-4), and satisfaction were compared.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 37
- Chronic interstitial cystitis
- Bladder Pain Syndrome
- Acute cystitis
- Bladder cancer
- Chronic prostatitis
- Bladder stone
- Stress incontinence
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description With Hunner's ulcer Pentosan Polysulphate Pentosan Polysulfate 100 mg Without Hunner's ulcer Pentosan Polysulphate Pentosan Polysulfate 100 mg
- Primary Outcome Measures
Name Time Method improvement of lower urinary tract symptoms Three months 1 if symptoms improved, 0 if not
bladder wall thickness Three months 0.3 over 3 mm 1 under 3 mm,
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (2)
Hisar Intercontinental Hospital
🇹🇷Istanbul, Turkey
Basri Cakiroglu
🇹🇷Istanbul, Turkey