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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04658940
Study type Interventional
Source Acutus Medical
Contact
Status Completed
Phase N/A
Start date March 25, 2021
Completion date June 12, 2022

See also
  Status Clinical Trial Phase
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Recruiting NCT05777850 - High-Power Short-Duration Radiofrequency Ablation in Patients With Typical Atrial Flutter N/A
Completed NCT01401361 - Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along With EnSite Velocity Contact System Phase 3
Completed NCT00984204 - Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the Treatment of Typical Atrial Flutter (AFL) Phase 3
Withdrawn NCT01710150 - Pulmonary Vein Isolation To Reduce Future Risk Of Atrial Fibrillation In Patients Undergoing Typical Flutter N/A
Completed NCT01408485 - Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter N/A
Recruiting NCT00750711 - Typical Flutter Ablation:A Comparison of 4 mm Versus 2 mm Irrigated cathéters N/A
Recruiting NCT03867266 - Typical Atrial Flutter, Ablation Index and Point by Point Ablation
Not yet recruiting NCT06157437 - An Exploratory Study of Focal Pulse Ablation System in the Treatment of Typical Atrial Flutter N/A
Recruiting NCT04657055 - AcQBlate Force Sensing Ablation System EU Study for Atrial Flutter (AcQForce Flutter-EU) N/A