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Typical Atrial Flutter clinical trials

View clinical trials related to Typical Atrial Flutter.

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NCT ID: NCT04658940 Completed - Clinical trials for Typical Atrial Flutter

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

AcQForce AFL
Start date: March 25, 2021
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT01408485 Completed - Clinical trials for Typical Atrial Flutter

Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter

FLEXION-AFL
Start date: November 2011
Phase: N/A
Study type: Interventional

To demonstrate that ablation with the Therapy™ Cool Flex™ Irrigated Ablation System is effective in the treatment of typical atrial flutter (cavo-tricuspid dependent) and that its use does not result in an unacceptable risk of intra-procedural, serious cardiac adverse events.

NCT ID: NCT01401361 Completed - Clinical trials for Typical Atrial Flutter

Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along With EnSite Velocity Contact System

CONTACT_AFL
Start date: October 2011
Phase: Phase 3
Study type: Interventional

To demonstrate that the use of Contact Therapy™ Cool Path™ ablation catheter in conjunction with the EnSite Velocity Contact Technology for the treatment of typical atrial flutter - Does not result into unacceptable risk of intra-procedural composite serious adverse events and, - Does not affect efficacy of the ablation procedure The study will also evaluate the

NCT ID: NCT00984204 Completed - Clinical trials for Typical Atrial Flutter

Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the Treatment of Typical Atrial Flutter (AFL)

Start date: October 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate that ablation with the Therapy™ Cool Path™ Duo cardiac ablation system can eliminate typical atrial flutter and that its use does not result in an unacceptable risk of serious adverse events (SAE's).