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NOT YET RECRUITING
NCT06863220
NA

Intravesical Ozone Therapy for Interstitial Cystitis/Bladder Pain Syndrome

Sponsor: Medipol University

View on ClinicalTrials.gov

Summary

This randomized, double-blind, placebo-controlled trial evaluated the efficacy and safety of intravesical ozone therapy in 60 patients with interstitial cystitis (IC). Participants were assigned to ozone therapy, placebo, or standard care groups for 3 weeks, with follow-up at 6 weeks. The primary outcome was the change in O'Leary-Sant ICSI score. Secondary outcomes included VAS pain score, SF-36 physical health, and urinary frequency.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2025-06-01

Completion Date

2026-06-01

Last Updated

2025-04-27

Healthy Volunteers

No

Interventions

OTHER

Intravesical Ozone Therapy

Patients received 50 mL ozonated saline (20-40 µg/mL) intravesically twice weekly for 3 weeks.

OTHER

Placebo (Normal Saline)

Patients received 50 mL normal saline intravesically twice weekly for 3 weeks.

OTHER

Control

Patients continued standard care (e.g., oral pentosan polysulfate) without intravesical intervention.

Locations (1)

İstanbul Başakşehir Çam Ve Sakura Şehir Hastanesi

Istanbul, Turkey (Türkiye)