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Correlating Ic/Pbs Symptoms With Urine Biomarkers

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00817388
First Posted: January 6, 2009
Last Update Posted: June 7, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
William Beaumont Hospitals
  Purpose
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 Intervention
Interstitial Cystitis Pelvic Pain Other: No intervention

Study Type: Observational
Official Title: Correlating Ic/Pbs Symptoms With Urine Biomarkers

Resource links provided by NLM:


Further study details as provided by William Beaumont Hospitals:

Primary Outcome Measures:
  • To correlate IC/PBS symptoms with urine biomarkers [ Time Frame: 2 years ]

Biospecimen Retention:   Samples Without DNA
Urine specimen.

Enrollment: 26
Study Start Date: January 2009
Study Completion Date: May 2010
Primary Completion Date: May 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
1
patients will be asked to provide a urine specimen and complete a questionnaire.
Other: No intervention
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.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Patients with and without intersitial cystitis/painful pelvic pain will be asked to provide an urine specimen and complete a brief questionnaire.
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

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00817388


Locations
United States, Michigan
William Beaumont Hospital
Royal Oak, Michigan, United States, 48073
Sponsors and Collaborators
William Beaumont Hospitals
Investigators
Principal Investigator: Michael Chancellor, MD William Beaumont Hospitals
  More Information

Responsible Party: Michael Chancellor, MD, Beaumont Hospitals
ClinicalTrials.gov Identifier: NCT00817388     History of Changes
Other Study ID Numbers: 2008-294
First Submitted: January 5, 2009
First Posted: January 6, 2009
Last Update Posted: June 7, 2010
Last Verified: June 2010

Keywords provided by William Beaumont Hospitals:
Interstitial cystitis
pelvic pain

Additional relevant MeSH terms:
Pelvic Pain
Cystitis
Cystitis, Interstitial
Pain
Neurologic Manifestations
Signs and Symptoms
Urinary Bladder Diseases
Urologic Diseases