Correlating Ic/Pbs Symptoms With Urine Biomarkers

Sponsor
William Beaumont Hospitals (Other)
Overall Status
Completed
CT.gov ID
NCT00817388
Collaborator
(none)
26
1
15.9
1.6

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

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 Design

Study Type:
Observational
Actual Enrollment :
26 participants
Official Title:
Correlating Ic/Pbs Symptoms With Urine Biomarkers
Study Start Date :
Jan 1, 2009
Actual Primary Completion Date :
May 1, 2010
Actual Study Completion Date :
May 1, 2010

Arms and Interventions

Arm Intervention/Treatment
1

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

Other: No intervention
No intervention

Outcome Measures

Primary Outcome Measures

  1. To correlate IC/PBS symptoms with urine biomarkers [2 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 William Beaumont Hospital Royal Oak Michigan United States 48073

Sponsors and Collaborators

  • William Beaumont Hospitals

Investigators

  • Principal Investigator: Michael Chancellor, MD, William Beaumont Hospitals

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00817388
Other Study ID Numbers:
  • 2008-294
First Posted:
Jan 6, 2009
Last Update Posted:
Jun 7, 2010
Last Verified:
Jun 1, 2010
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 7, 2010