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Clinical Trials/JPRN-UMIN000006420
JPRN-UMIN000006420Completed未知

Efficacy and safety of anticholinergic agents applied for day-time or night-time - Efficacy and safety of anticholinergic agents applied for day-time or night-time

Jikei University School of Medicine0 sites100 target enrollmentStarted: November 1, 2011Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Enrollment
100

Study Overview

Brief Summary

There were no significant differences between the nighttime and daytime treatment of tolterodine in terms of the adverse events such as thirsty in OAB patients. However, the limitation of this study is a few registrated number of patient (n=10), so that further stufy will be needed to clalify this point.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to 100years-old (—)
Sex
All

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1.Urinary retention has occured through the latest 1 year. 2.Post voied residual urine volume is more than 100ml. 3.The treatment has been already done. 4.Patients have sleep disturbance. 5.Patients have irregular life styles. 6.Patients have inhibited diseases for the use of anticholinergic agents.

Investigators

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