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Shock-Less Study

The purpose of this quality improvement study is to allow Medtronic and participating investigators to better address the quality of care patients receive by assessing the utilization of shock reduction programming features.
Principal Investigator: Ashish Sadhu, MD
Sponsor: Medtronic, Inc.
Enrollment Status: Open

BRADYCARE

Advanced BRADYCARrdia Device Feature Utilization and Clinical Outcomes

The purpose of this study is to evaluate the usage of advanced features and diagnostics in patients with St. Jude Medical pacemakers. The secondary aim of the study is to learn more about the progressive clinical outcomes in the general pacemaker patient population.
Principal Investigator: Ashish Sadhu, MD
Sponsor: St. Jude Medical
Enrollment Status: Closed

RATE Registry

Registry of Atrial Tachyarrhythmia/Atrial Fibrillation Episodes in the Cardiac Rhythm Management Device Population

The purpose of this registry is to produce a prospective, outcome-oriented registry to document the prevalence of AT/AF in the CRM population by using the Advanced AT/AF Diagnostics in select St. Jude Medical devices.
Principal Investigators: Ashish Sadhu, MD, Nathan Laufer, MD
Sponsor: St. Jude Medical
Enrollment Status: Open

Cardiac Ablation System

Clinical Evaluation of Contact™ Therapy™ Cool Path™ Cardiac Ablation System in Conjunction With EnSite Velocity Contact™ Technology for the Treatment of Typical Atrial Flutter (CONTACT AFL)

This will be a prospective, multi-center and non-randomized study. All enrolled patients who meet the eligibility criteria will receive ablation therapy for typical atrial flutter using the Contact Therapy™ Cool Path™ Cardiac Ablation System. Historical data from published (PMA P060019 Cool Path) , reported (IDE G090109 Cool Path Duo) and published literature on Atrial Flutter RF ablation studies is used to determine performance goals for primary study endpoints and derive the sample size.
Co-Investigators: Ashish Sadhu, MD
Sponsor: St. Jude Medical
Enrollment Status: Coming Soon