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NCT06100770 · ClinicalTrials.gov registry record

Aveir AR Coverage With Evidence Development (CED) Study

A clinical trial of Bradycardia and Arrhythmia, sponsored by Abbott Medical Devices.

Recruiting
Registry status
586
Enrollment target
1
Study location

NCT06100770 is a study of Bradycardia and Arrhythmia that is actively recruiting participants, run by Abbott Medical Devices. The registered enrollment target is 586 participants, below the 4,393-participant average among 29 other Bradycardia trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06100770, a study of Bradycardia and Arrhythmia, is actively recruiting participants, sponsored by Abbott Medical Devices.

RECRUITING
Registry status
586 participants
Enrollment target
1
Study location

Study Summary

The purpose of this coverage with evidence development (CED) study is to evaluate complications and long-term health outcomes of the single-chamber Aveir Atrial Leadless Pacemaker device (aka Aveir™ AR LP system).

Conditions Studied

Bradycardia Arrhythmia Cardiac Pacemaker

Interventions

  • DEVICE Aveir AR Leadless Pacemaker
  • DEVICE Single-chamber atrial transvenous pacemaker

Study Locations (1)

California

  • Abbott - Sylmar

Trial Details

FieldValue
Enrollment Target 586 participants
Start Date 2024-01-18
Est. Completion 2031-01

Sponsor

Abbott Medical Devices

261 total trials

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What the Registry Record Tells You About NCT06100770

The ClinicalTrials.gov registry entry for NCT06100770 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 586 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,393-participant average among 29 other Bradycardia trials with a reported enrollment target (87% lower). The listed sponsor is Abbott Medical Devices, which has 261 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Bradycardia appearing as the primary indexed condition, and to 2 interventions - of which Aveir AR Leadless Pacemaker is the first listed.

NCT06100770 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT06100770 about?

NCT06100770 is a clinical study titled "Aveir AR Coverage With Evidence Development (CED) Study". The purpose of this coverage with evidence development (CED) study is to evaluate complications and long-term health outcomes of the single-chamber Aveir Atrial Leadless Pacemaker device (aka Aveir™ AR LP system).

What is the current status of trial NCT06100770?

This trial is currently recruiting. The enrollment target is 586 participants. The study started on 2024-01-18. Estimated completion is 2031-01.

What conditions does trial NCT06100770 study?

This clinical trial studies the following conditions: Bradycardia, Arrhythmia, Cardiac Pacemaker.

What interventions are being tested in trial NCT06100770?

The interventions under investigation include: Aveir AR Leadless Pacemaker (DEVICE), Single-chamber atrial transvenous pacemaker (DEVICE).

Who is sponsoring clinical trial NCT06100770?

This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06100770 being conducted?

This trial has 1 study location across California. 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.