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Bryophyllum Pinnatum Versus Solifenacin Versus Placebo for Overactive Bladder (BryoSoliP)

Primary Purpose

Overactive Bladder, Urge Urinary Incontinence

Status
Terminated
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
Bryophyllum
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overactive Bladder focused on measuring Female, Postmenopause

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • OAB (>8 micturitions/24 hours, associated with urge symptoms)
  • postmenopausal women
  • cystoscopy to exclude a bladder carcinoma or carcinoma in situ
  • written and oral informed consent

Exclusion Criteria:

  • urinary tract infection in an intermittent catheter asservated sample (>1000 bacterias/ml)
  • intake of bladder affecting drugs like anticholinergics, diuretics, muscle relaxing medications and phytotherapeutics in the last three months
  • neurological conditions such as stroke, multiple sclerosis, spinal cord injury or Parkinsons's disease
  • postvoid residual volume ≥100 ml
  • lactose intolerance
  • contraindication for Solifenacin

Sites / Locations

  • Gynecologic Department, University Hospital Zurich
  • Gynecology Department, University Hospital Zurich

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Placebo Comparator

Experimental

Arm Label

Bryophyllum

Placebo

Solifenacin

Arm Description

50% in 350mg Lactose, 2-2-2

Lactose 350mg, 2-2-2

10mg in 350mg Lactose, 2-2-2

Outcomes

Primary Outcome Measures

Change of the micturition frequency
assessment of the voiding frequency in the 3-day bladder at visit 2,3,4,5,6

Secondary Outcome Measures

Changes in quality of life parameters
assessment with quality of life and symptom burden questionnaires at visit 2,3,4,5,6 (questionnaires ICIQ-OAB and KHQ)
Voiding diary parameters
3-day bladder diary returned at visit 2,3,4,5,6
Assessments of the patient's compliance
drug intake protocol and counting of the returned tablets
Assessment of AE/SAE
AE/SAE protocol

Full Information

First Posted
April 25, 2014
Last Updated
October 24, 2017
Sponsor
University of Zurich
Collaborators
PD Dr. med. Verena Geissbühler, Prof. pharm. Ursula von Mandach, Dr. med. David Scheiner, Dr. med. Matthias Werner
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1. Study Identification

Unique Protocol Identification Number
NCT02129816
Brief Title
Bryophyllum Pinnatum Versus Solifenacin Versus Placebo for Overactive Bladder
Acronym
BryoSoliP
Official Title
Treatment of Patients With Overactive Bladder With Bryophyllum Pinnatum Versus Solifenacinsuccinat Versus Placebo: Multicenter, Prospective, Double-blind Randomized, Placebo-controlled Cross-over Study, Phase III Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Terminated
Study Start Date
May 2014 (undefined)
Primary Completion Date
April 20, 2016 (Actual)
Study Completion Date
July 9, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
Collaborators
PD Dr. med. Verena Geissbühler, Prof. pharm. Ursula von Mandach, Dr. med. David Scheiner, Dr. med. Matthias Werner

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Overactive bladder (OAB) is an enigmatic condition that is treated symptomatically with anticholinergic drugs (gold standard 2013). In a clinical pilot study was found to be a trend for a higher reduction of the micturition frequency in the Bryophyllum pinnatum group - treated with chewing tablets containing 50% of dried BP leaf press juice - than in the placebo group (n=20, p=0.064) Hypothesis: To test the superior effectivity of Bryophyllum versus Placebo in the treatment of OAB with the needed number (Purpose 1) and to assess in an experimental arm the side effects of BP in comparison to the standard drug (Vesicare) in a clincial trial (Purpose 2).
Detailed Description
In a US nation-wide survey, lower urinary tract symptoms are one of the strongest predictors that patients will seek complementary and alternative medicine (CAM) care. In comparison to general gynecological patients, urogynecological patients are particularly prone to seek help in CAM. Moreover out of the different CAM options, herbal medication is one of the most preferred treatments. However, the effectiveness of CAM regarding OAB has not yet been adequately and objectively evaluated. Therefore, it is timely and essential to elucidate the mode of action as well as to prove efficacy of herbal treatments by a translational approach including comprehensive in vitro experimentation and randomized controlled clinical trials. Bryophyllum pinnatum and specially the flavonoid components have shown a muscle relaxing effect on porcine bladder strips. Study Design: Multicenter, prospective, double-blind randomized, placebo-controlled cross-over study, phase III to test the superiority of Bryophyllum pinnatum (BP) over placebo in the treatment of overactive bladder. In this cross-over trial a total of 30 patients is needed to proof the superiority of BP over placebo (5 randomization blocs, each 6 patients). Each patient gets each of the three study drugs (BP, Solifenacin, Placebo) in a double-blind randomization. The number of patients was calculated in a post-hoc analysis based on the primary endpoint of a previous study (reduction of micturition rates/24hours; 9.5 (SD2.2) before and 7.8 (SD1.2) after Bryophyllum versus 9.3 (SD1.8) before and 9.1(SD1.6) after placebo), under the assumption of a normal data distribution and a power of 80% a patient number of 2x20. Plus 10% for non-parametric tests in the case of a non-normal distribution (Wilcoxon) were added, what generated a number of 2x22 patients. In order to facilitate an equality in the randomization, the investigator choose a cross-over design. Due to the length of the study time, the drop-out rate was risen from 10 to 20% what yielded under the assumption of a equal block randomization the number of 30 patients. Additionally, an explorative arm containing the standard medication Vesicare was inserted, as this is of great clinical interest. For this explorative comparative arm are no existing data that would allow to do a power calculation. This follow-up study will give a compelling answer on the efficacy or non-efficacy of BP as well as the safety of BP in respect to placebo and possible answers of its position regarding the standard medication Vesicare.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overactive Bladder, Urge Urinary Incontinence
Keywords
Female, Postmenopause

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bryophyllum
Arm Type
Active Comparator
Arm Description
50% in 350mg Lactose, 2-2-2
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Lactose 350mg, 2-2-2
Arm Title
Solifenacin
Arm Type
Experimental
Arm Description
10mg in 350mg Lactose, 2-2-2
Intervention Type
Drug
Intervention Name(s)
Bryophyllum
Other Intervention Name(s)
dried leave press juice, provided by Weleda AG, Arlesheim, Switzerland
Primary Outcome Measure Information:
Title
Change of the micturition frequency
Description
assessment of the voiding frequency in the 3-day bladder at visit 2,3,4,5,6
Time Frame
participants will be followed for the duration of the study, an expected average of 35 weeks
Secondary Outcome Measure Information:
Title
Changes in quality of life parameters
Description
assessment with quality of life and symptom burden questionnaires at visit 2,3,4,5,6 (questionnaires ICIQ-OAB and KHQ)
Time Frame
participants will be followed for the duration of the study, an expected average of 35 weeks
Title
Voiding diary parameters
Description
3-day bladder diary returned at visit 2,3,4,5,6
Time Frame
participants will be followed for the duration of the study, an expected average of 35 weeks
Title
Assessments of the patient's compliance
Description
drug intake protocol and counting of the returned tablets
Time Frame
participants will be followed for the duration of the study, an expected average of 35 weeks
Title
Assessment of AE/SAE
Description
AE/SAE protocol
Time Frame
participants will be followed for the duration of the study, an expected average of 35 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: OAB (>8 micturitions/24 hours, associated with urge symptoms) postmenopausal women cystoscopy to exclude a bladder carcinoma or carcinoma in situ written and oral informed consent Exclusion Criteria: urinary tract infection in an intermittent catheter asservated sample (>1000 bacterias/ml) intake of bladder affecting drugs like anticholinergics, diuretics, muscle relaxing medications and phytotherapeutics in the last three months neurological conditions such as stroke, multiple sclerosis, spinal cord injury or Parkinsons's disease postvoid residual volume ≥100 ml lactose intolerance contraindication for Solifenacin
Facility Information:
Facility Name
Gynecologic Department, University Hospital Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland
Facility Name
Gynecology Department, University Hospital Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
23218404
Citation
Betschart C, von Mandach U, Seifert B, Scheiner D, Perucchini D, Fink D, Geissbuhler V. Randomized, double-blind placebo-controlled trial with Bryophyllum pinnatum versus placebo for the treatment of overactive bladder in postmenopausal women. Phytomedicine. 2013 Feb 15;20(3-4):351-8. doi: 10.1016/j.phymed.2012.10.007. Epub 2012 Dec 4.
Results Reference
result

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Bryophyllum Pinnatum Versus Solifenacin Versus Placebo for Overactive Bladder

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