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Pentosan Polysulfate Treatment's Effectiveness

Retrospective Evaluation of the Effectiveness of Oral Pentosan Polysulfate Treatment in the Improvement of Chronic Interstitial Cystitis Symptoms

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05744908
Enrollment
37
Registered
2023-02-27
Start date
2018-01-01
Completion date
2023-01-10
Last updated
2025-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Interstitial Cystitis

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.

Interventions

OTHERPentosan Polysulphate

300mg 3 times a day

Sponsors

Hisar Intercontinental Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

two models: with and without Hunner's ulcer

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Chronic interstitial cystitis * Bladder Pain Syndrome

Exclusion criteria

* Acute cystitis * Bladder cancer * Chronic prostatitis * Bladder stone * Stress incontinence

Design outcomes

Primary

MeasureTime frameDescription
bladder wall thicknessThree months0.3 over 3 mm 1 under 3 mm,
improvement of lower urinary tract symptomsThree months1 if symptoms improved, 0 if not

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026