This is a prospective pilot study, with a recruitment goal of 60 patients. Patients who are female, above the age of 18, and with a diagnosis of IC/BPS based on clinical criteria and O'Leary Sant ICPI and ICSI scores undergoing cystoscopy, hydrodistention and bladder biopsy will be included. The bladder biopsies will be evaluated for TLR4 expression, and sent for histological assessment of mast cell count. Additionally, data will be collected at baseline, day of surgery, day 7, day 14 and day 28. Data will include validated questionnaires, lower urinary tract symptoms, and recorded pain medication use.
Study Type
OBSERVATIONAL
Enrollment
60
Hahnemann Urogynecology
Philadelphia, Pennsylvania, United States
RECRUITINGToll-like Receptor 4 protein analysis
Determine Toll-like Receptor 4 protein expression with western blot
Time frame: 1 year
Toll-like Receptor 4 mRNA expression in bladder biopsy
Determine Toll-like Receptor 4 mRNA expression with quantitative polymerase chain reaction
Time frame: 1 year
Toll-like Receptor 4 distribution and localization evaluation
Determine Toll-like Receptor 4 distribution and localization with immunohistochemistry
Time frame: 1 year
Bladder symptom evaluation
Utilize O'Leary Sant Interstitial Cystitis Symptom and Problem Indices to evaluate subjective bladder symptom changes
Time frame: 28 days
Vaginal symptoms evaluation
Utilize pelvic floor impact questionnaire-7 to evaluate vaginal and pelvic symptoms
Time frame: 28 days
Female sexual function
Use female sexual function index questionnaire to evaluate female sexual function
Time frame: 28 days
Interstitial cystitis Flares
Patients will record bladder pain scores and changes in urinary urgency with the bladder diary to evaluate flares following cystoscopy, hydrodistention
Time frame: 28 days
Patient satisfaction
Use Global response assessment questionnaire
Time frame: 28 days
Bladder symptom evaluation
Utilize questionnaire: pelvic floor impact questionnaire-7
Time frame: 28 days
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