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NCT06056271 · ClinicalTrials.gov registry record

Clinical and Healthcare Outcomes From Real-World Use in the United States of a Companion AI During AF Ablation

A clinical trial of Atrial Fibrillation, sponsored by Volta Medical.

Recruiting
Registry status
400
Enrollment target
4
Study locations

NCT06056271 is a study of Atrial Fibrillation that is actively recruiting participants, run by Volta Medical. The registered enrollment target is 400 participants, below the 2,995-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (87% lower). The trial reports 4 study locations across 4 states.

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The verdict

NCT06056271, a study of Atrial Fibrillation, is actively recruiting participants, sponsored by Volta Medical.

RECRUITING
Registry status
400 participants
Enrollment target
4
Study locations

Study Summary

Observational, multi-center, clinical device registry for US patients with a primary goal to observe the clinical outcomes in patients who are mapped with Volta Medical's VX1 or AF-Xplorer systems during AF ablation procedures.

Conditions Studied

Atrial Fibrillation

Interventions

  • DEVICE AF Ablation

Study Locations (4)

Illinois

  • Endeavor Health - Evanston

Kansas

  • Kansas City Cardiac Arrhythmia Research LLC - Overland Park

New York

  • Northwell Health - New York

Ohio

  • Ohio State University - Columbus

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2024-03-19
Est. Completion 2027-12

Sponsor

Volta Medical

3 total trials

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What the Registry Record Tells You About NCT06056271

The ClinicalTrials.gov registry entry for NCT06056271 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,995-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (87% lower). The listed sponsor is Volta Medical, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Atrial Fibrillation appearing as the primary indexed condition, and to 1 intervention - of which AF Ablation is the first listed.

NCT06056271 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Illinois, Kansas, New York.

Frequently Asked Questions

What is clinical trial NCT06056271 about?

NCT06056271 is a clinical study titled "Clinical and Healthcare Outcomes From Real-World Use in the United States of a Companion AI During AF Ablation". Observational, multi-center, clinical device registry for US patients with a primary goal to observe the clinical outcomes in patients who are mapped with Volta Medical's VX1 or AF-Xplorer systems during AF ablation procedures.

What is the current status of trial NCT06056271?

This trial is currently recruiting. The enrollment target is 400 participants. The study started on 2024-03-19. Estimated completion is 2027-12.

What conditions does trial NCT06056271 study?

This clinical trial studies the following conditions: Atrial Fibrillation.

What interventions are being tested in trial NCT06056271?

The interventions under investigation include: AF Ablation (DEVICE).

Who is sponsoring clinical trial NCT06056271?

This trial is sponsored by Volta Medical, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06056271 being conducted?

This trial has 4 study locations across Illinois, Kansas, New York, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.