Correlating Ic/Pbs Symptoms With Urine Biomarkers

Completed

• Conditions: Interstitial Cystitis; Pelvic Pain
• Interventions: Other: No intervention

• Registration Number: NCT00817388
• Lead Sponsor: William Beaumont Hospitals

Brief Summary

Completion of a brief survey tool and providing an urine specimen. The study purpose is to improve our understanding of interstitial cystitis and painful pelvic syndrome.

Detailed Description

The purpose of the study is to improve our understanding of the IC/PBS and develop new treatments. Participation in the study will allow us to compare clinical information, obtained by completion of a brief survey, with substances found in the a urine specimen that is donated to the Beaumont Biobank.

Study Timeline

• Study Start: 2009-01
• Study First Submitted: 2009-01-05
• Study First Submitted QC: 2009-01-05
• Study First Posted: 2009-01-06
• Primary Completion: 2010-05
• Study Completion: 2010-05
• Status Verified: 2010-06
• Last Update Submitted: 2010-06-04
• Last Update Posted: 2010-06-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
1	No intervention	patients will be asked to provide a urine specimen and complete a questionnaire.

Primary Outcome Measures

Name	Time	Method
To correlate IC/PBS symptoms with urine biomarkers	2 years

Trial Locations

Locations (1)

William Beaumont Hospital; 🇺🇸 Royal Oak, Michigan, United States