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OpenTrials
Completed

NCT Number: NCT00817388

Correlating Ic/Pbs Symptoms With Urine Biomarkers

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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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion:

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

Exclusion:

  • Unable to complete questionnaires and/or give informed consent

Treatment and study plan

No intervention

Other

No intervention

Primary outcomes

  1. To correlate IC/PBS symptoms with urine biomarkers

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Corewell Health East

Other

Registry information

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Jan 6, 2009
Registry last updated
Jun 7, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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