Overactive bladder is a chronic and devastating condition in the aging population. Approximately 33 million people in the United States suffer from overactive bladder (OAB) and associated urinary urge incontinence (UUI), a chronic medical condition that drastically impairs quality of life and results in an annual economic burden of $66 billion. The psychological aspects of this chronic voiding dysfunction are particularly devastating; patients have increased incidences of depression, social isolation and sleep deprivation. Given that the incidence of OAB increases with advancing age, the prevalence of the condition and the total economic burden will continue to rise as the baby boomer population ages. Despite the high social and economic burden, a convenient, safe and effective treatment has yet to be realized. Recently, a minimally invasive neuromodulation device that provides percutaneous tibial nerve stimulation (PTNS) of the afferent sacral nerve, Congentix?s Urgent PC, has shown clinical success; however, this device requires weekly in-clinic treatments as well as repeated placement of an electrode into the posterior tibial nerve, both of which are cost prohibitive and challenging for patient adherence. Implantable neurostimulators (RENOVA iStim and eCoin?) are also under development, but these devices require a surgical procedure and, accordingly, initial clinical studies have had high complication rates, with a second surgery often required to address these adverse events. To meet the need for a safe, effective, comfortable, and easy-to-use treatment for OAB, TheraNova has developed an inexpensive, convenient device that enables non-invasive tibial nerve stimulation at home. Previously, we demonstrated that subjects treated with this system achieved reductions in the mean number of voids, the mean number of voids with moderate to severe urgency, and the mean number of UUI events. The goals of the parent Phase II award are to determine the effectiveness of our system versus a sham control treatment in a home-use, pivotal clinical study. In the parent award, we are conducting a clinical study to identify a well-blinded sham control treatment (Specific Aim 1). We will also validate the treatment effectiveness and durability for mitigating urinary urge incontinence compared to the sham control in a pivotal trial (Specific Aim 2). In the Diversity Supplement, we have assigned TheraNova?s Software Engineer, Ms. Maitreyee Mittal, an engineering leadership role in the project. She will lead the software development efforts for the TranStim device in the pivotal clinical trial, which will be focused on mobile app development. The app will be used by participants to log urinary voiding data, the primary data collection means in the study and a critical component of the study?s success. Ms. Mittal will also oversee all device manufacturing efforts and assist with device troubleshooting. The proposed work for Ms. Mittal will be performed within the overall scope of the parent award.

Public Health Relevance

Overactive bladder is a chronic medical condition that significantly diminishes the quality of life for many elderly patients. Commercially available neurostimulation therapies for overactive bladder are efficacious, however, they are limited in clinical use due to their invasive and cumbersome nature. We propose a novel, non-invasive, peripheral nerve stimulation device for in-home treatment of overactive bladder.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Small Business Innovation Research Grants (SBIR) - Phase II (R44)
Project #
3R44AG058272-03S2
Application #
10219001
Study Section
Program Officer
Salive, Marcel
Project Start
2017-12-01
Project End
2021-04-30
Budget Start
2020-11-15
Budget End
2021-04-30
Support Year
3
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Theranova, LLC
Department
Type
DUNS #
621187249
City
San Francisco
State
CA
Country
United States
Zip Code
94107