Clinical TrialID 7778

Effectiveness of Oral Boldo in Women With Overactive Bladder

NCT06162065

Urinary Bladder, Overactive

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Trial: 1Herb: 1Links: 1
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Record Fields

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Clinical Trial Id
7778
Evidence Id
7778
Core Evidence Id
7778
Source Clinical Trial Id
7771
Herb2 Clinical Trial Id
HBCT007771
Nct Id
NCT06162065
Title
Effectiveness of Oral Boldo in Women With Overactive Bladder
Status
Enrolling_By_Invitation
Phase
Phase 1
Study Result
No
Study Condition
Urinary Bladder, Overactive
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Intervention
DRUG: Oxybutynin Pill|DIETARY_SUPPLEMENT: Boldo supplement
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Single
Intervention Purpose
Treatment
Gender
Female
Age
Adult
Enrollment
10
Outcome Measure
Urinary symptoms, Using a urinary chart, measure urinary frequency and intervals., 1 month|Bladder Control Self-Assessment Questionnaire, measure the presence of urinary urgency and urine leakage along with the level of discomfort this produces, 1 month|MiniBESTest, Balance systems evaluation test (anticipatory, reactive postural control, sensory orientation, dynamic gait), 1 month
Sponsor Collaborator
Universidad de Valparaiso|Uro Medical Corporation
Funded By
OTHER
Location
Clínica Uromed, Santiago, Región Metropolitana, Chile
Other Id
118/2023
Start Date
2023-11-01
Primary Completion Date
2024-01-31
Completion Date
2024-03-30
First Posted
2023-12-08
Results First Posted
Last Update Posted
2023-12-08
Study Document
Study Url
https://clinicaltrials.gov/study/NCT06162065
Title Cn
Title En
Effectiveness of Oral Boldo in Women With Overactive Bladder
Bilingual Status
semi_complete