Are you a female with urinary pain, urgency and frequency?
If you are a female with symptoms of interstitial cystitis/bladder pain syndrome (IC/BPS), you may be eligible to participate in a clinical research study.
If you have symptoms of interstitial cystitis/bladder pain syndrome (IC/BPS), you may be eligible to participate in a clinical research study.
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If you are a female between the ages of 18 and 85, with urinary frequency, urgency and pelvic discomfort or pain for at least six months, you may be eligible to participate in a clinical research study.
Can I Participate?
You may be eligible to participate in this research study if you are:
A female
Between the ages of 18-85
Experiencing symptoms of IC/BPS (urinary frequency, urgency and pelvic discomfort or pain) for at least six months
Why Should I Participate?
Participating in this study will give you access to quality care at no cost. Your participation is critical to help improve the care we can give future patients as we learn more about IC/BPS, improve treatments and help with better diagnosis.
What's Involved?
If you meet the criteria to be included in the study, you will be scheduled to have:
Twice weekly treatment sessions for eight weeks
Phone or mail monitoring every six months, up to five times after treatment completion
Any treatment will be at no cost to you, a stipend will be provided for study participation. Expected study duration is eight weeks of active treatment with up to two years of follow-up.
