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F15 Recharge Free Axonics SNM System Clinical Study
NCT06186765 · View on ClinicalTrials.gov ↗
Study Summary
Multicenter, prospective, non randomized, single arm evaluation of patients with overactive bladder (OAB) and/or fecal incontinence (FI) employing the Axonics recharge free SNM System.
Conditions Studied
Interventions
- DEVICE Axonics SNM System (Model 4101)
Study Locations (16)
Other
- Erasmus Medical Center — Rotterdam
- Queen Elizabeth Hospital — Birmingham
- Bristol Urological Institute — Bristol
- University College London Hospital — London
- Northern General Hospital — Sheffield
Florida
- Florida Gulf Clinical Research — Bradenton
- East Coast Institute of Research — Jacksonville
- Florida Bladder Institute — Naples
Connecticut
- Hartford Healthcare — Waterford
Georgia
- Atrium Health — Macon
Minnesota
- Minnesota Urology — Coon Rapids
Nebraska
- Adult Pediatric Urology & Urogynecology — Omaha
New York
- Columbia University Medical Center — New York
Oregon
- The Oregon Clinic — Portland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 144 participants |
| Start Date | 2023-12-08 |
| Est. Completion | 2027-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06186765
The ClinicalTrials.gov registry entry for NCT06186765 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 144 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Axonics, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Urinary Urge Incontinence (UUI) appearing as the primary indexed condition, and to 1 intervention — of which Axonics SNM System (Model 4101) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06186765 reports 16 study locations spanning 10 distinct geographic areas — top geographies include Other, Florida, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06186765 about?
NCT06186765 is a clinical study titled "F15 Recharge Free Axonics SNM System Clinical Study". Multicenter, prospective, non randomized, single arm evaluation of patients with overactive bladder (OAB) and/or fecal incontinence (FI) employing the Axonics recharge free SNM System.
What is the current status of trial NCT06186765?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 144 participants. The study started on 2023-12-08. Estimated completion is 2027-03.
What conditions does trial NCT06186765 study?
This clinical trial studies the following conditions: Urinary Urge Incontinence (UUI), Urinary Frequency (UF), Fecal Incontinence (FI). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06186765?
The interventions under investigation include: Axonics SNM System (Model 4101) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06186765?
This trial is sponsored by Axonics, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06186765 being conducted?
This trial has 16 study locations across Connecticut, Florida, Georgia, Minnesota, Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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