Feasibility of Parasacral Transcutaneous Electrical Nerve Stimulation PTENS for Voiding Dysfunction in Peds Population
Primary Purpose
Overactive Bladder, Voiding Disorders, Incontinence, Urinary
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
parasacral transcutaneous electrical nerve stimulation (PTENS)
Standard Urotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Overactive Bladder
Eligibility Criteria
Inclusion Criteria:
- Toilet trained (age 6) to age 17
- Diagnosis of urinary dysfunction, voiding dysfunction, overactive bladder, urgency incontinence, nocturnal enuresis. (These patients may also have an element of bowel dysfunction; however, we will not include a patient who had ONLY bowel dysfunction and NOT a voiding dysfunction).
Exclusion Criteria:
- Known neurologic diagnosis - such as myelomeningocele, caudal regression
- Known seizure disorder
- Age < 6 or > 17
- Lack of follow-up within 6 months of treatment
- Pacemaker, vagal nerve stimulator, or other implanted electrical device
- Intolerance of electrical nerve stimulation
- Pregnancy
- Implanted metal hardware
- Open sores or wounds over the sacral area
- Currently catheterizing for bladder drainage
- Known anatomic lower urinary tract abnormality (may be congenital or iatrogenic)
- Bowel only voiding dysfunction (Constipation ICD-10 K59.00)
- Non-English speaking families
- Families with health literacy precluding completion of questionnaires and voiding diaries
- Concurrent use of anticholinergics, alpha blockers or beta agonists for urologic treatments
- Untreated urinary tract infection
Sites / Locations
- University of Utah/Primary Children's Pediatric Urology
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Standard Urotherapy
Standard Urotherapy + PTENS
Arm Description
Patients who meet eligibility criteria who will be counselled on standard recommendations for bladder management.
Patients who meet eligibility criteria who will be counselled on standard recommendations for bladder management AND use parasacral percutaneous TENS as additional treatment.
Outcomes
Primary Outcome Measures
Dysfunctional Voiding Symptom Score
At week 6 a Dysfunctional Voiding Scoring System Score. Descriptive statistics will be used to analyze these data in comparison to pre-study scores.
As stated above, Dysfunctional Voiding Symptom Score is a validated clinical questionnaire designed to quantify the severity of pediatric voiding dysfunction on a scale of 0 (non-existent) to 30 (most severe).
Voiding Diary and the Number of Episodes of Incontinence Per Day
48-hour Voiding Diary and Nighttime Wetting log will be repeated and evaluated. This was added as a separate primary outcome as it is separate from the Dysfunctional Voiding Symptom Score. The voiding diary will be used to evaluate the number of episodes of incontinence per day and descriptive statistics will be used to compare this to pre-study numbers.
Secondary Outcome Measures
Secondary Outcome. Review of Adverse Events.
Confirmation of safety and identification of potential adverse events. We will review all data for potential adverse events.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04570605
Brief Title
Feasibility of Parasacral Transcutaneous Electrical Nerve Stimulation PTENS for Voiding Dysfunction in Peds Population
Official Title
Feasibility of Home Parasacral Transcutaneous Electrical Nerve Stimulation (PTENS) for the Voiding Dysfunction in the Pediatric Population: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
June 1, 2020 (Actual)
Study Completion Date
July 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Utah
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Pilot study for determining feasibility of home parasacral transcutaneous electrical nerve stimulation in treatment of urinary urgency and incontinence.
Detailed Description
Overactive bladder (OAB) is the most common voiding dysfunction in children1. While many children may outgrow these issues, for some these symptoms persists and can lead to emotional, social, behavioral and physical problems. Multiple treatments exist for OAB but rarely is there guaranteed success. Many behavioral and lifestyle treatments involve a significant time investment and office visits on the part of the patient and family. Furthermore, medication therapy is often associated with bothersome side effects and is discontinued, even despite efficacy2. As such, treatments with potentially less adverse effects, often used in adult urology, are making their way into the pediatric urology practice. These include intravesical botulinum toxin injections, sacral nerve stimulation (SNS) and percutaneous tibial nerve stimulation (PTNS).
PTNS, first cleared by the United States Food and Drug Administration (FDA) in 2011 for adult use, has evolved into transcutaneous nerve stimulation in the pediatric population; obviating the need for needles during treatment. Studies suggest mixed efficacy in electric nerve stimulation for overactive bladder in the pediatric population, owing largely to the marked heterogeneity in treatment protocols. While some researchers follow the traditional tibial nerve pathway, others take a cue from SNS and target the parasacral area, while still others rely on signaling from even further peripheral nerves to modulate bladder overactivity 3-5. Perhaps further contributing to the disparate data is the varying treatment schedules used. Some centers perform treatments daily, others weekly, others twice or thrice a week. Similarly, some physicians recommend twenty-minute treatments, while others thirty or even sixty minutes. The majority of studies rely on an office-based treatment model, while a few have explored in home treatments 3-5. In the United States, there has been no study examining the feasibility or efficacy of home parasacral transcutaneous electric nerve stimulation (PTENS) on pediatric voiding dysfunction.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overactive Bladder, Voiding Disorders, Incontinence, Urinary
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized controlled trial
Masking
Participant
Masking Description
patients will be randomized to standard urotherapy or urotherapy + PTENS
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Standard Urotherapy
Arm Type
Active Comparator
Arm Description
Patients who meet eligibility criteria who will be counselled on standard recommendations for bladder management.
Arm Title
Standard Urotherapy + PTENS
Arm Type
Experimental
Arm Description
Patients who meet eligibility criteria who will be counselled on standard recommendations for bladder management AND use parasacral percutaneous TENS as additional treatment.
Intervention Type
Device
Intervention Name(s)
parasacral transcutaneous electrical nerve stimulation (PTENS)
Intervention Description
electrode patches placed on skin of lower back just above each side of the gluteal cleft (parasacral) and attached to TENS unit at specific settings three times a week for 30 minutes for 12 weeks.
Intervention Type
Other
Intervention Name(s)
Standard Urotherapy
Intervention Description
standard behavioral therapy recommendations including timed voiding, fluid intake recommendations and bowel management recommendations including videos instructing patients and parents on these issues. This is current standard of care.
Primary Outcome Measure Information:
Title
Dysfunctional Voiding Symptom Score
Description
At week 6 a Dysfunctional Voiding Scoring System Score. Descriptive statistics will be used to analyze these data in comparison to pre-study scores.
As stated above, Dysfunctional Voiding Symptom Score is a validated clinical questionnaire designed to quantify the severity of pediatric voiding dysfunction on a scale of 0 (non-existent) to 30 (most severe).
Time Frame
week 6
Title
Voiding Diary and the Number of Episodes of Incontinence Per Day
Description
48-hour Voiding Diary and Nighttime Wetting log will be repeated and evaluated. This was added as a separate primary outcome as it is separate from the Dysfunctional Voiding Symptom Score. The voiding diary will be used to evaluate the number of episodes of incontinence per day and descriptive statistics will be used to compare this to pre-study numbers.
Time Frame
week 6, week 12
Secondary Outcome Measure Information:
Title
Secondary Outcome. Review of Adverse Events.
Description
Confirmation of safety and identification of potential adverse events. We will review all data for potential adverse events.
Time Frame
Week 6 through Week 12
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Toilet trained (age 6) to age 17
Diagnosis of urinary dysfunction, voiding dysfunction, overactive bladder, urgency incontinence, nocturnal enuresis. (These patients may also have an element of bowel dysfunction; however, we will not include a patient who had ONLY bowel dysfunction and NOT a voiding dysfunction).
Exclusion Criteria:
Known neurologic diagnosis - such as myelomeningocele, caudal regression
Known seizure disorder
Age < 6 or > 17
Lack of follow-up within 6 months of treatment
Pacemaker, vagal nerve stimulator, or other implanted electrical device
Intolerance of electrical nerve stimulation
Pregnancy
Implanted metal hardware
Open sores or wounds over the sacral area
Currently catheterizing for bladder drainage
Known anatomic lower urinary tract abnormality (may be congenital or iatrogenic)
Bowel only voiding dysfunction (Constipation ICD-10 K59.00)
Non-English speaking families
Families with health literacy precluding completion of questionnaires and voiding diaries
Concurrent use of anticholinergics, alpha blockers or beta agonists for urologic treatments
Untreated urinary tract infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Glen A Lau, MD
Organizational Affiliation
University of Utah
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Utah/Primary Children's Pediatric Urology
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84112
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Individual participant data will be stored on password protected computers in the facility and collected data will be entered in a REDCap database. Individual participant data will not be shared with any individuals other than the study personnel as only these individuals will have access to the data.
Citations:
PubMed Identifier
28089606
Citation
de Paula LIDS, de Oliveira LF, Cruz BP, de Oliveira DM, Miranda LM, de Moraes Ribeiro M, Duque RO, de Figueiredo AA, de Bessa J Jr, Netto JMB. Parasacral transcutaneous electrical neural stimulation (PTENS) once a week for the treatment of overactive bladder in children: A randomized controlled trial. J Pediatr Urol. 2017 Jun;13(3):263.e1-263.e6. doi: 10.1016/j.jpurol.2016.11.019. Epub 2016 Dec 21. Erratum In: J Pediatr Urol. 2021 Jun;17(3):e1.
Results Reference
background
PubMed Identifier
10958730
Citation
Farhat W, Bagli DJ, Capolicchio G, O'Reilly S, Merguerian PA, Khoury A, McLorie GA. The dysfunctional voiding scoring system: quantitative standardization of dysfunctional voiding symptoms in children. J Urol. 2000 Sep;164(3 Pt 2):1011-5. doi: 10.1097/00005392-200009020-00023.
Results Reference
background
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Feasibility of Parasacral Transcutaneous Electrical Nerve Stimulation PTENS for Voiding Dysfunction in Peds Population
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