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Intravaginal Electrical Stimulation in Idiopathic Overactive Bladder

Primary Purpose

Idiopathic Overactive Bladder, Electrical Stimulation, Bladder Training

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Electrical stimulation (IVES)
Bladder Training
Sponsored by
Pamukkale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Overactive Bladder

Eligibility Criteria

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

Inclusion Criteria:

  • Women over the age of 18 with clinical diagnosis of idiopathic OAB
  • Urodynamically diagnosed detrusor overactivity
  • The strength of pelvic floor muscle 3/5 and more
  • Able to give written, informed consent
  • Able to understand the procedures, advantages and possible side effects
  • Willing and able to complete the voiding diary and QoL questionnaire

Exclusion Criteria:

  • History of conservative therapy (BT, ES) for OAB within 3 months
  • Previously treated with antimuscarinics (within 4 weeks)
  • Pregnancy or intention to become pregnant during the study
  • Current vulvovaginitis or urinary tract infections or malignancy
  • History of urogynecological surgery within 3 months
  • Anatomic structural disorders of genital region that could not allow to apply the vaginal probe
  • Having stage 2 or more according to the pelvic organ prolapse quantification
  • Cardiac pacemaker or implanted defibrillator
  • Neurogenic bladder, signs of neurologic abnormalities at objective examination; history of the peripheral or central neurologic pathology
  • Ultrasonographic evidence of residual urine volume more than 100 ml
  • Allergy to condom or lubricant gel that is used with perineometer/vaginal probe

Sites / Locations

  • Hakan Alkan

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Active Comparator

Arm Label

Group 1: Bladder Training - Control group

Group 2: Bladder Training+Intra Vaginal Electrical Stimulation

Arm Description

Specific goals are to correct faulty habit patterns of frequent urination, improve control over bladder urgency, prolong voiding intervals, increase bladder capacity, reduce incontinence episodes and restore patient confidence in controlling bladder function

IVES was performed in lithotomy position via Enraf Nonius Myomed 632 device with a vaginal probe. IVES sessions were performed three times in a week, for 8 weeks. Every session lasted 20 minutes. The intervention comprised a 24-session treatment program of ES. The stimulation parameters were frequency at 10 Hz, a 5-10s work-rest cycle and 100 ms pulse width. The symmetric biphasic pulse wave could be delivered over a range of 0-100 mA. The intensity was controlled according to patients' discomfort level feedback

Outcomes

Primary Outcome Measures

incontinence episodes-incontinence related outcomes measures
Patients with a 50% or greater reduction in incontinence episodes were consider positive responders (number of voiding per day)

Secondary Outcome Measures

frequency of voiding-incontinence related outcomes measures
it was used frequency from data with a bladder diary (number of voiding per day)
nocturia frequency- incontinence related outcomes measures
it was used nocturia from data with a bladder diary (number of voiding per night)
incontinence related quality of life questionnaire
(IIQ-7) (score)

Full Information

First Posted
May 12, 2020
Last Updated
May 24, 2021
Sponsor
Pamukkale University
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1. Study Identification

Unique Protocol Identification Number
NCT04389307
Brief Title
Intravaginal Electrical Stimulation in Idiopathic Overactive Bladder
Official Title
Bladder Training With and Without Intravaginal Electrical Stimulation in Women With Idiopathic Overactive Bladder: A Prospective Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
June 1, 2020 (Actual)
Primary Completion Date
December 1, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Pamukkale University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Overactive bladder (OAB) is a symptom complex defined as urgency, with or without urge urinary incontinence (UUI), usually with frequency and nocturia, in the absence of urinary tract infection. Currently, a wide range of therapeutic options exist for the treatment of OAB. These include first-line conservative (physical) therapies which focus on electrical stimulation (ES) and behavioral therapies such as lifestyle modifications, bladder training (BT), pelvic floor muscle training with or without biofeedback, second-line therapies which are pharmacologic, and third-line therapies which either neuromodulate or chemodenervate the bladder. In clinical practice, BT and Intravaginal ES (IVES) are frequently used together in the treatment of women with OAB, but the evidences/results of the combined (BT+IVES) use of these two treatment options are so rare that they can be neglected in the literature. There is only one study including BT+ES treatment arm (one of the four treatment arms) in women with idiopathic OAB in the literature. In a study, BT+ES was not found to be effective both from BT alone and from the untreated control group. While interpreting the results of this study, it should be take into consideration that patients treated received relatively few treatment sessions (nine treatment sessions, once weekly) in this study. In addition, in the light of authors clinical experience, the investigators think that this issue is still open for research. Moreover, there is no recommendation on conservative combinations in the guidelines due to insufficient data. This study is the first prospective randomized controlled trial that compares the efficacy of BT and BT plus IVES in women with idiopathic OAB. In this study, the investigators aimed to evaluate the efficacy of BT with and without IVES on incontinence-related QoL and clinical parameters in women with idiopathic OAB.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Overactive Bladder, Electrical Stimulation, Bladder Training

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1: Bladder Training - Control group
Arm Type
Other
Arm Description
Specific goals are to correct faulty habit patterns of frequent urination, improve control over bladder urgency, prolong voiding intervals, increase bladder capacity, reduce incontinence episodes and restore patient confidence in controlling bladder function
Arm Title
Group 2: Bladder Training+Intra Vaginal Electrical Stimulation
Arm Type
Active Comparator
Arm Description
IVES was performed in lithotomy position via Enraf Nonius Myomed 632 device with a vaginal probe. IVES sessions were performed three times in a week, for 8 weeks. Every session lasted 20 minutes. The intervention comprised a 24-session treatment program of ES. The stimulation parameters were frequency at 10 Hz, a 5-10s work-rest cycle and 100 ms pulse width. The symmetric biphasic pulse wave could be delivered over a range of 0-100 mA. The intensity was controlled according to patients' discomfort level feedback
Intervention Type
Other
Intervention Name(s)
Electrical stimulation (IVES)
Intervention Description
IVES sessions were performed three times in a week, for 8 weeks. Every session lasted 20 minutes. The intervention comprised a 24 session treatment program of IVES.
Intervention Type
Other
Intervention Name(s)
Bladder Training
Intervention Description
Bladder Training
Primary Outcome Measure Information:
Title
incontinence episodes-incontinence related outcomes measures
Description
Patients with a 50% or greater reduction in incontinence episodes were consider positive responders (number of voiding per day)
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
frequency of voiding-incontinence related outcomes measures
Description
it was used frequency from data with a bladder diary (number of voiding per day)
Time Frame
8 weeks
Title
nocturia frequency- incontinence related outcomes measures
Description
it was used nocturia from data with a bladder diary (number of voiding per night)
Time Frame
8 weeks
Title
incontinence related quality of life questionnaire
Description
(IIQ-7) (score)
Time Frame
8 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women over the age of 18 with clinical diagnosis of idiopathic OAB Urodynamically diagnosed detrusor overactivity The strength of pelvic floor muscle 3/5 and more Able to give written, informed consent Able to understand the procedures, advantages and possible side effects Willing and able to complete the voiding diary and QoL questionnaire Exclusion Criteria: History of conservative therapy (BT, ES) for OAB within 3 months Previously treated with antimuscarinics (within 4 weeks) Pregnancy or intention to become pregnant during the study Current vulvovaginitis or urinary tract infections or malignancy History of urogynecological surgery within 3 months Anatomic structural disorders of genital region that could not allow to apply the vaginal probe Having stage 2 or more according to the pelvic organ prolapse quantification Cardiac pacemaker or implanted defibrillator Neurogenic bladder, signs of neurologic abnormalities at objective examination; history of the peripheral or central neurologic pathology Ultrasonographic evidence of residual urine volume more than 100 ml Allergy to condom or lubricant gel that is used with perineometer/vaginal probe
Facility Information:
Facility Name
Hakan Alkan
City
Denizli
State/Province
None Selected
ZIP/Postal Code
20100
Country
Turkey

12. IPD Sharing Statement

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Intravaginal Electrical Stimulation in Idiopathic Overactive Bladder

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