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Completed Not applicable Interventional Results available

AcQBlate Force Sensing Ablation System US IDE for Atrial Flutter (AcQForce Flutter)

ClinicalTrials.gov ID: NCT04658940

Public ClinicalTrials.gov record NCT04658940. 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 Oct 20, 2026, 3:28 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 Acutus Medical AcQForce Flutter clinical study is a prospective, multi-center, non-randomized global study designed to demonstrate the safety and effectiveness of the AcQBlate Force Sensing Ablation System in the ablation management of symptomatic cavotricuspid isthmus dependent atrial flutter.

Study identification

NCT ID
NCT04658940
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Acutus Medical
Industry
Enrollment
115 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
Mar 25, 2021 (Actual)
Primary completion
May 12, 2022 (Actual)
Completion
Jun 12, 2022 (Actual)
Last update posted
Sep 28, 2023

2021 – 2022

United States locations

U.S. sites
20
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
AZ Cardiovascular Research Center Phoenix Arizona 85016 —
Arrhythmia Research Group Jonesboro Arkansas 72401 —
John Muir Health Concord California 94520 —
San Diego Cardiac Center Medical Group, Inc. San Diego California 92123 —
Hartford Hospital Hartford Connecticut 06102 —
BayCare Heath Clearwater Florida 33756 —
Celebration Hospital Orlando Florida 32803 —
Bayfront Health St. Petersburg Florida 33701 —
St Alphonsus Health System Boise Idaho 83704 —
Kansas City Heart Rhythm Institute Overland Park Kansas 66211 —
Baptist Lexington Medical Center Lexington Kentucky 40503 —
MedStar Health Research Institute Hyattsville Maryland 80784 —
Adventist Healthcare | White Oak Medical Center Silver Spring Maryland 20904 —
Adventist Healthcare, Inc Silver Spring Maryland 20904 —
Weill Cornell New York New York 10021 —
Ohio State Med Ctr Columbus Ohio 43201 —
ProMedica Physician Cardiology Toledo Ohio 43615 —
Penn State Health Hershey Pennsylvania 17033-0850 —
Lancaster General Hospital Lancaster Pennsylvania 17603 —
Presbyterian Medical Center Philadelphia Pennsylvania 19104 —

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04658940, 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 Sep 28, 2023 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04658940 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →