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Sensory Processing in Subjects With Painful Bladder Syndrome

NCT00903643 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 34

Last updated 2014-07-22

No results posted yet for this study

Summary

The purpose of this study is to determine if clinically relevant subsets exist in patients meeting the diagnosis of Painful Bladder Syndrome (PBS). Subsets suggest differential responses to treatments and if verified, this will be important for the stratification of patients in clinical studies related to PBS.

Conditions

  • Painful Bladder Syndrome

Interventions

OTHER

Physical examination

Physical examination and multiple questionnaires will be administered

Sponsors & Collaborators

  • Washington University Early Recognition Center

    collaborator OTHER

  • University of Alabama at Birmingham

    lead OTHER

Principal Investigators

  • Timothy Ness, MD, PhD · University of Alabama at Birmingham

Eligibility

Min Age
19 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-05-31
Primary Completion
2014-06-30
Completion
2014-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00903643 on ClinicalTrials.gov