Correlating Ic/Pbs Symptoms With Urine Biomarkers

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

26 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-01-31

Study Completion Date

2010-05-31

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Interstitial Cystitis Pelvic Pain

Study Groups

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1

patients will be asked to provide a urine specimen and complete a questionnaire.

No intervention

Intervention Type OTHER

No intervention

Interventions

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No intervention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Men and women with interstitial cystitis/painful bladder syndrome greater than 18 years old
2. Male and female controls without a history of IC/PBS diagnosis

Exclusion:

1\. Unable to complete questionnaires and/or give informed consent

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes