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ACTIVE NOT RECRUITING NA

Prospective Feasibility Study Evaluating EchoMark LP Placement and EchoSure Measurements for Subjects Requiring Arteriovenous Fistulae

NCT04896476 · View on ClinicalTrials.gov ↗

Study Summary

Multi-center trial to assess the feasibility and safety of the EchoMark LP and the EchoMark diagnostic ultrasound system for assessing AV fistula blood flow, diameter, and depth.

Interventions

  • DEVICE EchoMark / EchoSure

Study Locations (4)

Alabama

  • Trinity Research Group — Dothan

Arizona

  • SKI Vascular Center — Peoria

Michigan

  • Michgan Vascular Center — Flint

North Carolina

  • Surgical Specialist of Charlotte — Charlotte

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2022-01-21
Est. Completion 2025-06-06
Phase NA

Sponsor

Sonavex

29 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04896476

The ClinicalTrials.gov registry entry for NCT04896476 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 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sonavex, which has 29 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Kidney Diseases appearing as the primary indexed condition, and to 1 intervention — of which EchoMark / EchoSure 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: NCT04896476 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Alabama, Arizona, Michigan. 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 NCT04896476 about?

NCT04896476 is a clinical study titled "Prospective Feasibility Study Evaluating EchoMark LP Placement and EchoSure Measurements for Subjects Requiring Arteriovenous Fistulae". Multi-center trial to assess the feasibility and safety of the EchoMark LP and the EchoMark diagnostic ultrasound system for assessing AV fistula blood flow, diameter, and depth.

What is the current status of trial NCT04896476?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2022-01-21. Estimated completion is 2025-06-06.

What conditions does trial NCT04896476 study?

This clinical trial studies the following conditions: Kidney Diseases, Arteriovenous Fistula. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04896476?

The interventions under investigation include: EchoMark / EchoSure (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04896476?

This trial is sponsored by Sonavex, which has 29 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04896476 being conducted?

This trial has 4 study locations across Alabama, Arizona, Michigan, North Carolina. 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