Acute Pudendal Nerve Stimulation On Leak Point Pressure In Women Urodynamic Early Feasibility Study

Not Applicable

Terminated

• Conditions: Urinary Incontinence
• Interventions: Diagnostic Test: Urodynamic testing with and without pudendal nerve stimulation

• Registration Number: NCT05128682
• Lead Sponsor: William Beaumont Hospitals

Brief Summary

The purpose of this study is tp evaluate the changes in stress induced Urethral Leak Point Pressures (LPP) and other urodynamic measurements in response to acute pudendal nerve stimulation (PNS) in patients with a pre-existing implanted urological neurostimulator stimulating the pudendal nerve.

Detailed Description

Patients with a neurostimulator implanted at the pudendal nerve will be enrolled and undergo urodynamic testing. Before testing, study staff will provide an oral antibiotic (to reduce the risk of infection) and adjust the stimulation settings with a goal to increase urethral pressure from baseline by at lest 20cm H2O, without causing the patient discomfort/distress. These settings will be used throughout urodynamics. Before filling the bladder, a urethral pressure profile study will be completed 3 times with stimulation off, then 3 times with stimulation on. Leak point pressure (LPP) testing will then be completed. The patient's bladder will be filled following standard urodynamic testing protocol. Filling will be paused every 50-100mL to complete LPP assessment. Subjects will be asked to complete a light cough, medium cough, forceful cough, and Valsalva maneuver (in that order). Detrusor pressure will be measured at each event, and staff will document whether or not a leak was elicited. This will be completed with stimulation off, then with stimulation on, as the bladder is filled. Once the subject reports a strong urge to void, urethral pressure profile assessment will be completed again: 3 times with stimulation off, then 3 times with stimulation on. Once urodynamic testing is complete and the patient's bladder is emptied, a measurement of urethral pressure will be completed with stimulation off, then during 5 seconds of stimulation, then again with stimulation off.

Study Timeline

• Study First Submitted: 2021-09-22
• Study First Submitted QC: 2021-11-16
• Study First Posted: 2021-11-22
• Study Start: 2022-05-24
• Primary Completion: 2022-07-27
• Study Completion: 2022-09-07
• Results First Submitted: 2023-03-20
• Status Verified: 2023-05
• Results First Submitted QC: 2023-05-12
• Last Update Submitted: 2023-05-12
• Results First Posted: 2023-05-16
• Last Update Posted: 2023-05-16

Recruitment & Eligibility

• Status: TERMINATED
• Sex: Female
• Target Recruitment: 4

Inclusion Criteria

• Women between the ages of 18 and 85 years old, inclusive.
• Implanted with a neurostimulation device for at least 3 months prior to consent (Medtronic Interstim neurostimulator models 3023, 3058, 97810, or similar).
• Implanted with a tined lead that is placed and functionable at the pudendal nerve (Medtronic model 3889 or similar).
• Is capable of understanding clinical study procedures and giving informed consent.
• Willing and able to visit the clinic for the UDT evaluation (study procedure)

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Exclusion Criteria

• Medically unstable at time of study and unsafe to undergo urodynamic testing as determined by the investigator.
• History of bladder cancer.
• History of pelvic radiotherapy.
• Active gross hematuria.
• Active symptomatic urinary tract infection (UTI)
• Active symptomatic uncontrolled bladder instability as determined by the investigator.
• History or symptoms of cystocele, enterocele, or rectocele of grade 3 or 4. Per the medical record or as determined by the investigator.
• Presence of an artificial urinary sphincter.
• Women who are pregnant and/or have given birth in the previous 12 months
• Any medical condition that would interfere with the patient's ability to comply with the protocol and/or may affect the outcome of this study or safety of the subject as determined by the investigator
• BMI greater than 39.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Urodynamic testing with and without pudendal nerve stimulation	Urodynamic testing with and without pudendal nerve stimulation	The neuromodulation settings of the implanted device will be adjusted to deliver acute simulation. Urodynamic testing (UDT) will be completed by filling the bladder and observing for urinary leakage. The assessment will be completed with the stimulation sets turned off and then turned on. At the end of the UDT the settings will be returned to the previously set therapeutic values. The neuromodulation settings constitute the "dose" and can include the voltage/current amplitude, frequency, pulse width, on time/off time duration and electrode polarity assignments. These parameters are limited by the available ranges of the approved neurostimulation device and will be adjusted during the study by the principal investigator to stay within the safe and comfortable levels for each individual study subject.

Primary Outcome Measures

Name	Time	Method
Pulse Amplitude Triggering Patient Sensation at First Verbally Reported Sensation.	After Visit 2 activities are complete. An average of 30 days after enrollment.	PNS final settings including: pulse amplitude, measured in mA, when subject first verbalizes sensation. Pulse amplitude is the amplitude of the electric pulses; measured in Milliamps (mA). This is a setting present on the neuromodulation device, it is not calculated.
Pulse Frequency Triggering Patient Sensation at First Verbally Reported Sensation.	After Visit 2 activities are complete. An average of 30 days after enrollment.	PNS final settings including: pulse frequencies, measured in Hz, when subject first verbalizes sensation.
Pulse Width Triggering Patient Sensation at First Verbally Reported Sensation.	After Visit 2 activities are complete. An average of 30 days after enrollment.	PNS final settings including: pulse widths, measured in µs, when the subject first verbalizes sensation.
Identification of All Study-related Adverse Events	After Visit 2 activities are complete. An average of 30 days after enrollment.	Safety and tolerability will be assessed in relation to the incidence of study related adverse events reported.
Changes in Leak Point Pressure (LPP) Upon Acute PNS	After Visit 2 activities are complete. An average of 30 days after enrollment.	Measurement of the change in LPP with acute PNS compared to without stimulation. To assess LPP, the urethral pressure increase will be calculated by subtracted pressure with and without stimulation at the "final setting". In cm water.

Secondary Outcome Measures

Name	Time	Method
Effect of Acute PNS on the Urethral Pressure Profile (UPP).	After Visit 2 activities are complete. An average of 30 days after enrollment.	Measure the maximum urethral closure pressure with and without programmed pudendal nerve stimulation. In cm water.; Urethral pressure profile is a test of the bladder neck, urethra, and urethral sphincters that is completed with urodynamic equipment. A small catheter is pulled at a constant rate from the bladder neck down the urethra to provide the functional length of the urethra and points of maximal urethral resistance at the urethral sphincter. It is a procedure used to measure the competency of the urethral sphincter (outflow resistance).
Effect of Acute PNS on Max Cystometic Capacity.	After Visit 2 activities are complete. An average of 30 days after enrollment.	Max cystometic capacity will be collected, with and without programmed PNS, the difference will be reported. In mL.
Effect of Acute PNS on Post Void Residual.	After Visit 2 activities are complete. An average of 30 days after enrollment.	Post void residual collected at end of UDT testing. Measured in mL.

Trial Locations

Locations (2)

Beaumont Hospital Royal Oak; 🇺🇸 Royal Oak, Michigan, United States

Beaumont Hospital - Royal Oak; 🇺🇸 Royal Oak, Michigan, United States