Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

A Real World Study of eCoin for Urgency Urinary Incontinence: Post Approval Evaluation (RECIPE)

NCT05685433 · View on ClinicalTrials.gov ↗

Study Summary

A prospective, multicenter, single-arm study to evaluate the safety and effectiveness of the eCoin® implanted tibial nerve stimulator in subjects with urgency urinary incontinence (UUI).

Interventions

  • DEVICE eCoin Tibial Nerve Stimulation

Study Locations (20)

California

  • University of California, Irvine — Irvine
  • AIR Research — Los Angeles
  • Stanford Health — Stanford

Alabama

  • Urology Centers of Alabama — Homewood
  • USA Health — Mobile

Iowa

  • The Iowa Clinic — Ankeny
  • University of Iowa — Iowa City

Kansas

  • University of Kansas Medical Center Research Institute, Inc — Kansas City
  • Cypress Medical Research — Wichita

Arkansas

  • Arkansas Urology — Little Rock

Florida

  • Urological Research Network Corp — Hialeah

Georgia

  • The Emory Clinic — Atlanta

Illinois

  • Rush University — Chicago

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2023-01-26
Est. Completion 2031-12
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05685433

The ClinicalTrials.gov registry entry for NCT05685433 describes a study currently listed as 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 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Valencia Technologies Corporation, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Overactive Bladder appearing as the primary indexed condition, and to 1 intervention — of which eCoin Tibial Nerve Stimulation 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: NCT05685433 reports 20 study locations spanning 15 distinct geographic areas — top geographies include California, Alabama, Iowa. 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 NCT05685433 about?

NCT05685433 is a clinical study titled "A Real World Study of eCoin for Urgency Urinary Incontinence: Post Approval Evaluation (RECIPE)". A prospective, multicenter, single-arm study to evaluate the safety and effectiveness of the eCoin® implanted tibial nerve stimulator in subjects with urgency urinary incontinence (UUI).

What is the current status of trial NCT05685433?

This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2023-01-26. Estimated completion is 2031-12.

What conditions does trial NCT05685433 study?

This clinical trial studies the following conditions: Overactive Bladder, Urge Incontinence, Urinary Urge Incontinence, Incontinence, Urinary. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05685433?

The interventions under investigation include: eCoin Tibial Nerve Stimulation (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05685433?

This trial is sponsored by Valencia Technologies Corporation, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05685433 being conducted?

This trial has 20 study locations across Alabama, Arkansas, California, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial