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临床试验/NCT04000763
NCT04000763已完成不适用

Superficial Peroneal Nerve Neuromodulation for Non-Obstructive Urinary Retention

Christopher J Chermansky, MD2 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2019年12月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
2
试验地点
2
主要终点
Number of catheterizations per subject in 24 hours.

研究概览

简要总结

Millions of Americans are suffering from underactive bladder (UAB). The impact of severe UAB, i.e. non-obstructive urinary retention (NOUR) on quality of life is significant because current treatment for non-obstructive urinary retention requires intermittent self-catheterization or an indwelling suprapubic catheter. Currently an effective drug for non-obstructive urinary retention does not exist. It is a therapeutic challenge for clinicians to successfully treat non-obstructive urinary retention. Sacral neuromodulation has been approved by the FDA since 1999 to treat non-obstructive urinary retention. It achieves >50% improvement in bladder emptying (reducing the frequency of self-catheterization or increasing voided volume) in just over half of the patients. Sacral neuromodulation requires surgical implantation of a stimulator and a lead with 4 electrodes. The surgery and implant are invasive and expensive, preventing a broad application of this effective therapy to many non-obstructive urinary retention patients. The goal of this study is to develop a novel non-invasive neuromodulation therapy for non-obstructive urinary retention as an alternative. Specifically, the investigators will explore the possibility to translate into humans a recent discovery in cats of an excitatory reflex from the superficial peroneal nerve to the bladder to treat non-obstructive urinary retention. Therefore, in this study the investigators propose to develop a non-invasive, transcutaneous neuromodulation therapy for non-obstructive urinary retention that can be administered at home.

详细描述

Hypothesis

Electrical stimulation of the superficial peroneal nerve using transcutaneous skin electrodes attached on the dorsal foot can treat non-obstructive urinary retention either by enhancing bladder sensation thereby reducing bladder volume needed for initiating voiding and/or by enhancing bladder contraction, thereby increasing voiding efficiency and reducing post-void residual (PVR) volume.

Rationale: The investigators conducted preliminary studies in cats that have demonstrated an excitatory reflex to the bladder elicited by stimulation of afferent axons in the superficial peroneal nerve. Activating this excitatory reflex in cats reduced bladder capacity (the minimal volume for initiating a micturition reflex), enhanced bladder contractions and overcame bladder inhibition emanating from somatic (tibial) afferent activation. Since the superficial peroneal nerve innervates the dorsal skin of the foot in humans, it can be stimulated non-invasively by skin surface electrodes. Transcutaneous stimulation of this nerve, should it prove efficacious, would likely be more acceptable to patients with non-obstructive urinary retention (NOUR) than invasive sacral neuromodulation therapy. Therefore, in this study, the investigators propose to test the superficial peroneal nerve neuromodulation in non-obstructive urinary retention patients.

Specific Aim: Determine the efficacy of superficial peroneal nerve stimulation (SPNS) in the treatment of patients with non-obstructive urinary retention using skin electrodes attached to the dorsal surface of the foot.

Rationale: Based on a preliminary discovery in cats, the investigators propose to further investigate the effect of superficial peroneal nerve stimulation (SPNS) on voiding efficiency, post-void residual (PVR) volume, and bladder capacity (voided volume + post-void residual) in patients with non-obstructive urinary retention. A reduced bladder capacity indicates more normal bladder filling sensations, thereby allowing voiding at more normal volumes. The investigators plan to test superficial peroneal nerve stimulation in 10 non-obstructive urinary retention patients by collecting voiding diary during a 3-week period. Baseline voiding diary will be collected during the first week before superficial peroneal nerve stimulation initiation. During the second week, superficial peroneal nerve stimulation will be administered to each patient for 3 hours/day before sleep and it will also be administered immediately prior and throughout each void. The 3-hour stimulation is designed to modulate bladder sensory pathways to enhance bladder sensation, thereby reducing the bladder volume required to initiate voiding. The acute stimulation during each void is designed to enhance bladder contraction, thereby increasing voiding efficiency and reducing post-void residual. During the third week, superficial peroneal nerve stimulation will not be applied, and a voiding diary will be collected to determine any post-stimulation effect. Since the superficial peroneal nerve is a cutaneous nerve innervating the skin of the dorsal foot, superficial peroneal nerve stimulation will be applied non-invasively by attaching skin surface electrodes to the dorsal side of the foot.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Able to provide informed consent
  • 18 years of age and older
  • Clinically diagnoses as non-obstructive urinary retention
  • Post Void Residual of 300 mL or greater
  • Currently using daily self-catheterization to empty the bladder
  • Capable of using the toilet independently without difficulty
  • Capable and willing to follow all study-related procedures

排除标准

  • Neurologic diagnosis (including diabetes mellitus)
  • Surgery within one year of screening for urinary outlet obstruction
  • Pregnant or planning to become pregnant during study duration
  • OnabotulinumtoxiA use in bladder or pelvic floor muscles with the past year
  • Pacemaker or implantable defibrillator
  • Current Urinary tract or vaginal infections
  • Current Interstim use
  • Current Percutaneous tibial nerve stimulation (PTNS) or transcutaneous electrical nerve stimulation (TENS) use in pelvis or back or legs
  • Investigational drug/ device therapy with the past 4 weeks,
  • Participation in any clinical investigation involving or impacting gynecologic or urinary function with the past 4 weeks,
  • Previous surgery of or damage to the foot or nerves in the foot and leg.

结局指标

主要结局

Number of catheterizations per subject in 24 hours.

时间窗: 3 weeks

Counted using a patient voiding diary both before and after superficial peroneal nerve stimulation.

Catheterized Post Void Residual volume

时间窗: 3 weeks

Calculated in millimeters both before and after peroneal nerve stimulation.

Volume of urine per void.

时间窗: 3 weeks

Calculated in millimeters both before and after peroneal nerve stimulation.

Bladder capacity

时间窗: 3 weeks

Calculated by adding the voided volume to the post residual catheterization volume, in milliliters

Number of voids per subject in 24 hours.

时间窗: 3 weeks

Counted using a patient voiding diary both before and after superficial peroneal nerve stimulation.

Bladder Voiding efficiency

时间窗: 3 weeks

Pre voiding and post voiding ratio that reflects bladder contractility

次要结局

  • Efficacy of Foot Stimulation(3 weeks)
  • Post-stimulation effect(1 week)

研究者

发起方
Christopher J Chermansky, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Christopher J Chermansky, MD

Assistant Professor

University of Pittsburgh

研究点 (2)

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