Clinical TrialID 524

Effectiveness of Bryophyllum in Nocturia-Therapy

NCT04480658

Nocturia|Sleep Disorder

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Record Fields

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Clinical Trial Id
524
Evidence Id
524
Core Evidence Id
524
Source Clinical Trial Id
507
Herb2 Clinical Trial Id
HBCT000507
Nct Id
NCT04480658
Title
Effectiveness of Bryophyllum in Nocturia-Therapy
Status
Completed
Phase
Study Result
No
Study Condition
Nocturia|Sleep Disorder
Study Type
Interventional
Study Design
Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Intervention
DRUG: Bryophyllum pinnatum 50 %, tablets into capsules (verum: 2x2capsules/day)
Intervention Allocation
Intervention Model
Single_Group
Intervention Mask
Intervention Purpose
Treatment
Gender
Female
Age
Adult, Older_Adult
Enrollment
50
Outcome Measure
Reduction of nocturia frequency, micturition protocol will be handed over during the baseline visit, it will be filled three days before the second visit in 1 week( therapy-start), follow-up control 3 weeks after medication intake and after the completed medication period \], 4 Weeks|Sleep-Quality., Pittsburgh Sleep Quality Index (PSQI; score 0-21) will be handed over during the baseline visit and will be filled three days before the second visit in 1 Week and three days after the therapy-end (after 3 Weeks). The global PSQI score is then calculated by totaling the seven component scores, providing an overall score ranging from 0 to 21, where lower scores denote a healthier sleep quality., 4 Weeks
Sponsor Collaborator
University of Zurich
Funded By
OTHER
Location
University of Hospital, Clinic for Gynecology, Zurich, 8091, Switzerland
Other Id
2017-01964
Start Date
2018-01-01
Primary Completion Date
2021-02-18
Completion Date
2022-01-14
First Posted
2020-07-21
Results First Posted
Last Update Posted
2022-01-19
Study Document
Study Url
https://clinicaltrials.gov/study/NCT04480658
Title Cn
Title En
Effectiveness of Bryophyllum in Nocturia-Therapy
Bilingual Status
semi_complete