a

Not Applicable

• Conditions: Interstitial cystitis/ Hypersensitive bladder syndrome

• Registration Number: JPRN-UMIN000008484
• Lead Sponsor: Department of Urology, Graduate school of medicine, University of Tokyo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-07-20
• Study Completion: 2013-03-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Not provided

Exclusion Criteria

a

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Average voided volume at four weeks of the drug administration.