The purpose of this study is to evaluate efficacy and safety of additional hyaluronic acid/chondroitin sulfate to transurethral resection of bladder ulcer in patient with interstitial cystitis.
This is a randomized, parallel, 6 month period study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Additional Hyaluronic acid/chondroitin sulfate instillation to the bladder
Asan medical center
Seoul, South Korea
Change of pain scores on the Visual Analogue Scale
Change of pain scores on the Visual Analogue Scale
Time frame: 1month, 3month, 6month
Duration of symptom improvement
Duration of symptom improvement
Time frame: 1month, 3month, 6month
Changes of frequency and urgency on voiding diary
Changes of frequency and urgency on voiding diary
Time frame: 1month, 3month, 6month
Change score of O'Leary-Sant Interstitial Cystitis questionnaire (IC-Q)
Change score of O'Leary-Sant Interstitial Cystitis questionnaire (IC-Q)
Time frame: 1month, 6month
Score of Global Response Assessment (GRA), Patient Global Assessment (PGA) score
Score of Global Response Assessment (GRA), Patient Global Assessment
Time frame: 6month
Occurrence of adverse event
Occurrence of adverse event
Time frame: 6month
Change score of Pelvic Pain and Urgency/Frequency Patient Symptom Scale(PUF)
Change score of Pelvic Pain and Urgency/Frequency Patient Symptom Scale
Time frame: 1month, 6month
Change score of EQ-5D Health Questionnaire
Change score of EQ-5D Health Questionnaire
Time frame: 1month, 6month
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Change score of Brief Pain Inventory-short form (BPI-sf)
Change score of Brief Pain Inventory-short form (BPI-sf)
Time frame: 1month, 6month