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NCT01819168 Clinical Trial

Antimuscarinic Treatment for Female Patients With Overactive Bladder Syndrome: Comparison of Daytime and Nighttime Dosing

Overactive Bladder Syndrome Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01819168
Other study ID # 102026-E
Secondary ID
Status Completed
Phase N/A
First received March 21, 2013
Last updated September 4, 2016
Start date March 2013
Est. completion date April 2016

Study information
Verified date February 2016
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial Summary

The aim of this retrospective study is to analyze if nighttime antimuscarincs may be more effective in treating patients with nocturia.

Recruitment information / eligibility
Status Completed
Enrollment 38
Est. completion date April 2016
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 99 Years
Eligibility Inclusion Criteria:

- patients who underwent tolterodine SR treatment once per day for 12 weeks in Department of Obstetrics & Gynecology in National Taiwan University Hospital and Far Eastern Memorial Hospital

Exclusion Criteria:

Study Design

Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
Taiwan Far Eastern Memorial Hospital Pan-Chiao, New Taipei

Sponsors (1)
Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary bladder diary To clarity any difference of reduction in the episodes of nocturia between these two groups. 3 months No
Secondary Frequency and Urgency To clarity any difference of reduction in the episodes of urinary frequency and urgency between these two groups. 3 months No
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