UnknownPhase 4NCT01312259
Clinical Efficacy of Changing the InterStim® Parameters in Patients With Interstitial Cystitis/Painful Bladder Syndrome
Studying Interstitial cystitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Pelvic and Sexual Health Institute
- Principal Investigator
- Kristene E Whitmore, MDDrexel University College of Medicine
- Intervention
- Changing the Interstim parameter of '' Frequency" in patients with Interstitial Cystitis(other)
- Enrollment
- 72 enrolled
- Eligibility
- 18-70 years · FEMALE
- Timeline
- 2011 – 2018
Study locations (1)
- Pelvic and Sexual Health Institute, Philadelphia, Pennsylvania, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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