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Pentosan Polysulfate Treatment's Effectiveness

Not Applicable
Completed
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
Inclusion Criteria
  • Chronic interstitial cystitis
  • Bladder Pain Syndrome
Exclusion Criteria
  • Acute cystitis
  • Bladder cancer
  • Chronic prostatitis
  • Bladder stone
  • Stress incontinence

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
With Hunner's ulcerPentosan PolysulphatePentosan Polysulfate 100 mg
Without Hunner's ulcerPentosan PolysulphatePentosan Polysulfate 100 mg
Primary Outcome Measures
NameTimeMethod
improvement of lower urinary tract symptomsThree months

1 if symptoms improved, 0 if not

bladder wall thicknessThree months

0.3 over 3 mm 1 under 3 mm,

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Hisar Intercontinental Hospital

🇹🇷

Istanbul, Turkey

Basri Cakiroglu

🇹🇷

Istanbul, Turkey

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