Aquarius Pilot Study to Evaluate the New Axonics Trial System
Purpose
Evaluation of the new Axonics External Trial System (ETS-02) in patients with overactive bladder (OAB) and/or fecal incontinence (FI).
Conditions
- Urinary Urge Incontinence (UUI)
- Urinary Frequency (UF)
- Fecal Incontinence (FI)
- Overactive Bladder (OAB)
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- 18 years or older - Provides written informed consent prior to trial procedures - Primary indication of OAB (UUI/UF) or chronic FI who are considered candidates for an Axonics PNE procedure as assessed by the physician per product IFU
Exclusion Criteria
- Any participant that the study Investigator deems to be a poor candidate for any reason, including, but not limited to, inability to complete a baseline bladder or bowel diary or to be compliant with study visits - Planned changes to current regimen of medications during the trial period that could impact bladder or bowel function - Current urinary tract mechanical obstruction (e.g., benign prostatic enlargement or urethral stricture) - Current symptomatic urinary tract infection (UTI)
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Patients diagnosed with OAB and/or FI who are candidates for Axonics SNM (PNE) procedure |
External trial system used evaluated whether patients with OAB or FI will be responsive to sacral neuromodulation. |
|
More Details
- Status
- Recruiting
- Sponsor
- Axonics, Inc.
Detailed Description
The trial system is used to determine if patients are responsive to sacral neuromodulation (SNM) prior to receiving the Axonics implantable neurostimulator (INS) which is approved for the treatment of OAB and FI. This study is evaluating the feasibility and safety of the new Axonics External Trial System (ETS-02) in patients with overactive bladder (OAB) and/or fecal incontinence (FI).