Correlating Ic/Pbs Symptoms With Urine Biomarkers

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00817388

Enrollment

Registered

2009-01-06

Start date

2009-01-31

Completion date

2010-05-31

Last updated

2010-06-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Interstitial Cystitis, Pelvic Pain

Keywords

Interstitial cystitis, pelvic pain

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.

Interventions

OTHERNo intervention

No intervention

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

Inclusion: 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

Design outcomes

Primary

Measure	Time frame
To correlate IC/PBS symptoms with urine biomarkers	2 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026