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Active, not recruiting Not applicable Interventional

Abbott Medical - VERITAS Study

ClinicalTrials.gov ID: NCT06707688

Public ClinicalTrials.gov record NCT06707688. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 2:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to evaluate the safety and effectiveness of Abbott's Amulet™ 2 Left Atrial Appendage (LAA) occluder device (Amulet 2 device) in patients who have non-valvular atrial fibrillation and who are at increased risk for stroke and systemic embolism and have appropriate rationale to seek a non-pharmacologic alternative to oral anticoagulation.

Study identification

NCT ID
NCT06707688
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Abbott Medical Devices
Industry
Enrollment
458 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 6, 2024
Primary completion
Nov 5, 2025
Completion
Aug 31, 2027
Last update posted
Aug 3, 2026

2024 – 2027

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Arizona Arrhythmia Research Group Phoenix Arizona 85016
Arrhythmia Research Group Jonesboro Arkansas 72401
Baptist Medical Center Jacksonville Florida 32207
AdventHealth Orlando Orlando Florida 32803
Northside Hospital Atlanta Georgia 30342
Kansas City Cardiac Arrhythmia Research Foundation Overland Park Kansas 66211
Henry Ford Providence Southfield Hospital Southfield Michigan 48075
Mayo Clinic Rochester Minnesota 55905
CHI Health Creighton University Medical Center-Bergan Mercy Omaha Nebraska 68124
NYU Langone Health New York New York 10016
Mount Sinai Hospital New York New York 10019
Roper Hospital Charleston South Carolina 29401
Trident Medical Center Charleston South Carolina 29406
Vanderbilt Heart & Vascular Institute Nashville Tennessee 37232
Texas Cardiac Arrhythmia Austin Texas 78705
Baylor Scott & White All Saints Medical Center Fort Worth Texas 76104
Vital Heart and Vein Humble Texas 77338
Baylor Scott & White - The Heart Hospital Plano Plano Texas 75093
Heart Rhythm Associates Shenandoah Texas 77380

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06707688, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 3, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06707688 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →