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A new device for interstitial cystitis is compared to inactive control to determine if it is safe and effective. The study lasts approximately 7 weeks with a 19-week follow-up period.
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Lead Sponsor
Watson Pharmaceuticals
NCT07391306 · IC, Interstitial Cystitis and Bladder Pain Syndrome, and more
NCT05737121 · Interstitial Cystitis, Bladder Pain Syndrome
NCT00389142 · Interstitial Cystitis, Bladder Pain Syndrome
NCT05726786 · Bladder Cancer, Interstitial Cystitis, and more
NCT05149573 · Interstitial Cystitis, Chronic Interstitial Cystitis, and more
Boulder, Colorado
Denver, Colorado
Farmington, Connecticut
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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