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Pilotstudie zur Anwendung eines pflanzlichen Kombinationspräparats bei Frauen mit Reizblase (Overactive Bladder-Syndrom).(Translation: Pilot-Study with a herbal combination in women suffering from the overactive bladder syndrome (irritable bladder)). - femina study

Active, not recruiting
Conditions
Frequent micturition and urinary urgency, as common in patients suffering from overactive bladder syndrome.
MedDRA version: 9.1Level: LLTClassification code 10059617Term: Overactive bladder
Registration Number
EUCTR2009-011418-68-DE
Lead Sponsor
GlaxoSmithKline Consumer Healthcare GmbH & Co. KG
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Recruiting
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

•Women aged = 18 = 60 years
•>= 8 micturions during 24 hours (average according diary over 3 days)
•>= 1 episode of urge or urge incontinence in 24 hours (average according diary over 3 days)
•overactive bladder symptoms consist since at least 3 months

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

•Diseases and conditions that may cause secondary irritable bladder or cause any other micturition complaints
•Bladder cancer
•Unexplained hematuria
•Severe renal diseases
•Severe hepatic diseases
•Known hypersensitivity to ingredients of the study medication

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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