Evaluation of the TheraNova Neuromodulation System to Provide Durable Relief of Overactive Bladder Symptoms
NCT05162833 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3
Last updated 2024-02-28
Summary
To evaluate the safety and durability of the TheraNova Neuromodulation System in overactive bladder (OAB) patients.
Conditions
Interventions
- DEVICE
-
TheraNova Neuromodulation Device
TENS device
Sponsors & Collaborators
-
Theranova, L.L.C.
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-02-20
- Primary Completion
- 2023-12-08
- Completion
- 2023-12-08
- FDA Device
- Yes
Countries
- United States
Study Locations
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