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

No results posted yet for this study

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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05162833 on ClinicalTrials.gov