Electromagnetic Stimulation for the Treatment of Urge Urinary Incontinence and Overactive Bladder (ELEC STIM)
Primary Purpose
Urinary Incontinence, Urge
Status
Terminated
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Electrical Field Stimulation Device
Sham Nerve Stimulation Device
Sponsored by
About this trial
This is an interventional treatment trial for Urinary Incontinence, Urge focused on measuring Urinary Incontinence, Urge, Peripheral Nerve Stimulation
Eligibility Criteria
Inclusion Criteria:
- Urinary Urge Incontinence
- Urinary Frequency
Exclusion Criteria:
- Primary complaint of Stress Incontinence
- Neurogenic bladder
- Overflow Incontinence
- Functional Incontinence
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Investigational Device
Sham Device
Arm Description
Treatment using electrical field stimulation of peripheral nerves
Control group using sham device to mimic sound and sensation of investigational device
Outcomes
Primary Outcome Measures
Reduction of incontinence episodes from baseline to follow-up greater for device arm than sham arm
Significant increase in the percentage of patients reporting a reduction in number of incontinence episodes per day for the investigational device vs. sham
No Serious Adverse Events or Unanticipated Adverse Device Effects
Freedom from Serious Adverse Events or Unanticipated Adverse Device Effects related to procedure and/or investigational device through follow-up
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01464372
Brief Title
Electromagnetic Stimulation for the Treatment of Urge Urinary Incontinence and Overactive Bladder
Acronym
ELEC STIM
Official Title
Electrical Field Stimulation for the Treatment of Urge Urinary Incontinence and Overactive Bladder - Version: 3.0 Dated 16 APR 2012.
Study Type
Interventional
2. Study Status
Record Verification Date
January 2013
Overall Recruitment Status
Terminated
Study Start Date
October 2011 (undefined)
Primary Completion Date
October 2012 (Actual)
Study Completion Date
January 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
EMKinetics, Inc
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to collect data on the safety and efficacy of using an electrical field stimulation device, compared to a sham (placebo) device, to treat urinary urgency, urinary frequency and urge incontinence.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence, Urge
Keywords
Urinary Incontinence, Urge, Peripheral Nerve Stimulation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
130 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Investigational Device
Arm Type
Experimental
Arm Description
Treatment using electrical field stimulation of peripheral nerves
Arm Title
Sham Device
Arm Type
Sham Comparator
Arm Description
Control group using sham device to mimic sound and sensation of investigational device
Intervention Type
Device
Intervention Name(s)
Electrical Field Stimulation Device
Intervention Description
Treatment with Electrical Field Stimulation Device
Intervention Type
Device
Intervention Name(s)
Sham Nerve Stimulation Device
Intervention Description
Use of the sham device
Primary Outcome Measure Information:
Title
Reduction of incontinence episodes from baseline to follow-up greater for device arm than sham arm
Description
Significant increase in the percentage of patients reporting a reduction in number of incontinence episodes per day for the investigational device vs. sham
Time Frame
One week after final treatment visit
Title
No Serious Adverse Events or Unanticipated Adverse Device Effects
Description
Freedom from Serious Adverse Events or Unanticipated Adverse Device Effects related to procedure and/or investigational device through follow-up
Time Frame
First treatment through follow-up (one week after last treatment)
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Urinary Urge Incontinence
Urinary Frequency
Exclusion Criteria:
Primary complaint of Stress Incontinence
Neurogenic bladder
Overflow Incontinence
Functional Incontinence
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kenneth Peters, MD
Organizational Affiliation
Birmingham Urologic Associates
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Scott MacDiarmid, MD
Organizational Affiliation
Alliance Urology Specialists
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Electromagnetic Stimulation for the Treatment of Urge Urinary Incontinence and Overactive Bladder
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