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Completed Phase 2 Interventional Results available

Efficacy and Safety Study of Uracyst to Treat Interstitial Cystitis/Painful Bladder Syndrome

ClinicalTrials.gov ID: NCT00919113

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00919113. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 14, 2026, 10:53 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Randomized, Double-Blind, Parallel Group Evaluation of the Effectiveness and Safety of Uracyst® Compared to Inactive Control in Subjects With Interstitial Cystitis/Painful Bladder Syndrome

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00919113
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Watson Pharmaceuticals
Industry
Enrollment
98 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2009 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Dec 2010 (Actual)
Last update posted
May 3, 2013

2009 – 2010

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Not listed Boulder Colorado 80304 —
Not listed Denver Colorado 80211 —
Not listed Farmington Connecticut 06032 —
Not listed Plantation Florida 33317 —
Not listed Wellington Florida 33414 —
Not listed Columbus Georgia 31904 —
Not listed Coeur d'Alene Idaho 83814 —
Not listed Evanston Illinois 60201 —
Not listed Melrose Park Illinois 60160 —
Not listed Royal Oak Michigan 48073 —
Not listed Las Vegas Nevada 89148 —
Not listed Englewood New Jersey 07601 —
Not listed Sewell New Jersey 08080 —
Not listed Woodlane New Jersey 08060 —
Not listed Albany New York 12206 —
Not listed Poughkeepsie New York 12601 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Oklahoma City Oklahoma 73104 —
Not listed Philadelphia Pennsylvania 19104 —
Not listed Mountlake Terrace Washington 98043 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00919113, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 3, 2013 · Synced Nov 14, 2026

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