Pulsed Electromagnetic Stimulation for Treatment of Overactive Bladder

To assess the initial safety and clinical feasibility of neuromodulation therapy in treating patients with documented overactive bladder. The specific aim is improved urinary frequency and urgency after 12 weeks of treatment

Study Overview

• Status: Terminated
• Conditions: Urinary Bladder, Overactive
• Intervention / Treatment: Device: MagPro R30

Detailed Description

Twenty to Forty patients with documented overactive bladder will receive 30 minutes of treatment one day a week for 12 weeks. Treatment will consist of stimulating the posterior tibial nerve in the area of the ankle with a pulsed electromagnetic field. Study treatments will be administered by a commercially available MagPro R30, with a cooled figure eight coil, and a surface electrode placed over the afferent pathway of the sacral nerve.

The specific aim is improved urinary frequency and urgency after 12 weeks of treatment.

Secondary goals.

• To estimate the extent to which the device will decrease the number of episodes of involuntary urine loss due to frequency/urgency in comparison to historical controls.
• To evaluate the potential of the device for improving patient quality of life as measured by a clinically validated scale, such as the Incontinence Quality of Life Instrument (I-QOL) or equivalent
• To periodically employ a micturition diary to record variables such as day/night urgency/frequency episodes, number of voids per day, severity of leaks, number of absorbent products used per day, etc.

• Study Type: Interventional
• Enrollment (Actual): 4
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • California
    • San Francisco, California, United States, 94122
      • UCSF Urology Faculty Practice

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• The patient is > 18 years old.
• The patient has ≥ 6 month history of documented overactive bladder.
• The patient has failed other conventional therapy (i.e.- Kegel exercises, biofeedback methodology, etc.).
• The patient is free of mechanical urethral obstruction as documented by cystoscopy or pressure flow criteria.
• The patient demonstrates an understanding of neuromodulation therapy, its benefits, and its potential risks.
• The patient is willing and able to keep accurate records of their voiding on the provided voiding diaries.
• The patient is willing and able to comply with the Study Protocol.
• The patient agrees to and is capable of answering a quality of life questionnaire.
• The patient has normal functioning of the upper urinary tract.
• The patient has an intact peripheral neurosensory system.
• If the patient is/was on pharmacologic treatment for urgency/frequency syndrome, a 10-day washout period prior to treatment must be completed.
• The patient has sufficient outlet resistance at the urinary sphincter (i.e.- the patient does not have intrinsic sphincter deficiency).

Exclusion Criteria:

• The patient is pregnant or intends to become pregnant during the course of the study. (Patients becoming pregnant during the course of the study will immediately be terminated from the study.) Warning: The effects of neuromodulation on a developing fetus are unknown
• The patient has an active urinary tract infection.
• The patient has abnormal cystoscopy, which is concerning for or indicative of malignancy.
• The patient has a urinary fistula.
• The patient has a bladder stone.
• The patient has had ankle injury or surgery which results inability to stimulate the tibial nerve or discomfort in using the foot cradle
• The patient has metal implant from surgery or a metallic foreign body in either leg below (distal to) the knee.
• The patient has cochlear implants.
• The patient has a hyperreflexic neurogenic bladder or urodynamically proven instability secondary to a known neurourologic cause (i.e.- stroke, Parkinson's, Multiple Sclerosis).
• The patient has had four or more urinary tract infections in the past year.
• The patient has a chronic disease or diminished mental capacity that, in the Principal Investigator's judgement, would impair their ability to successfully understand and comply with the protocol.
• The patient has a history of gross hematuria or glycosuria within the last year.
• The patient has chronic constipation (less than two (2) bowel movements per week).
• The patient has significant pathology that would compromise sphincter competency.
• The patient has uncontrolled diabetes.
• The patient has diagnosed peripheral neuropathy such as diabetes with peripheral nerve involvement.
• The patient has concomitant medical conditions that would limit the success of the procedure or confound study results, including but not limited to patients with nerve damage, pacemakers or implantable defibrillators.
• The patient is unable or unwilling to sign informed consent.
• The patient is on pharmacologic treatment that could affect bladder function.
• The patient has known moderate to severe ureteral reflux or hydronephrosis.
• The patient has severe urethral stricture(s).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Improved urinary frequency and urgency after 12 weeks of treatment.	12 weeks

Secondary Outcome Measures

Outcome Measure	Time Frame
To estimate the extent to which the device will decrease the number of episodes of involuntary urine loss due to frequency/urgency in comparison to historical controls	12 weeks
To evaluate the potential of the device for improving patient quality of life as measured by a clinically validated scale, such as the Incontinence Quality of Life Instrument (I-QOL) or equivalent	12 weeks
To periodically employ a micturition diary to record variables such as day/night urgency/frequency episodes, number of voids per day, severity of leaks, number of absorbent products used per day, etc	12 weeks

Collaborators and Investigators

• Sponsor: EMKinetics, Inc
• Investigators: Principal Investigator: Donna Y Deng, MD, UCSF Department of Urology

Study record dates

Study Major Dates

• Study Start: December 1, 2008
• Primary Completion (Actual): December 1, 2009
• Study Completion (Actual): April 1, 2010

Study Registration Dates

• First Submitted: December 8, 2008
• First Submitted That Met QC Criteria: December 8, 2008
• First Posted (Estimate): December 10, 2008

Study Record Updates

• Last Update Posted (Estimate): June 8, 2011
• Last Update Submitted That Met QC Criteria: June 6, 2011
• Last Verified: June 1, 2011

More Information

Terms related to this study

• Keywords: Overactive Bladder; Overactive Urinary Bladder; Bladder, Overactive; Overactive Detrusor; Detrusor, Overactive; Overactive Detrusor Function; Detrusor Function, Overactive
• Additional Relevant MeSH Terms: Urologic Diseases; Urinary Bladder Diseases; Lower Urinary Tract Symptoms; Urological Manifestations; Urinary Bladder, Overactive
• Other Study ID Numbers: EMK1208

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No