Clinical TrialID 525

Bryophyllum Versus Placebo for Overactive Bladder

NCT01127126

Overactive Bladder

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
525
Evidence Id
525
Core Evidence Id
525
Source Clinical Trial Id
508
Herb2 Clinical Trial Id
HBCT000508
Nct Id
NCT01127126
Title
Bryophyllum Versus Placebo for Overactive Bladder
Status
Completed
Phase
Phase 2
Study Result
No
Study Condition
Overactive Bladder
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Intervention
DRUG: Bryophyllum pinnatum, Placebo in form of Lactose
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Quadruple
Intervention Purpose
Treatment
Gender
Female
Age
Adult, Older_Adult
Enrollment
22
Outcome Measure
Reduction of micturition frequency/24h, micturition frequency measured with the micturition protocoll, micturition protocol three days before baseline visit and follow-up control 2 and 8 weeks after medication intake and 6 weeks after the completed medication period
Sponsor Collaborator
University of Zurich
Funded By
OTHER
Location
Department of Obstetrics and Gynecology, Zurich, 8091, Switzerland
Other Id
2009-0075/4
Start Date
2010-12
Primary Completion Date
2012-01
Completion Date
2012-01
First Posted
2010-05-20
Results First Posted
Last Update Posted
2012-01-19
Study Document
Study Url
https://clinicaltrials.gov/study/NCT01127126
Title Cn
Title En
Bryophyllum Versus Placebo for Overactive Bladder
Bilingual Status
semi_complete