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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00817388
Other study ID # 2008-294
Secondary ID
Status Completed
Phase N/A
First received January 5, 2009
Last updated June 4, 2010
Start date January 2009
Est. completion date May 2010

Study information

Verified date June 2010
Source William Beaumont Hospitals
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date May 2010
Est. primary completion date May 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

N/A


Intervention

Other:
No intervention
No intervention

Locations

Country Name City State
United States William Beaumont Hospital Royal Oak Michigan

Sponsors (1)

Lead Sponsor Collaborator
William Beaumont Hospitals

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To correlate IC/PBS symptoms with urine biomarkers 2 years No
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