WATCHMAN FLX™ Pro Left Atrial Appendage Closure Device with Alternative Post-Implant Monotherapy (SIMPLAAFY),
Role: Research Coordinator/Nurse,
Boston Scientific Corp.,
(02/2026 - 02/2027)
Status: Approved
ULTRASOUND-BASED RENAL SYMPATHETIC DENERVATION AS ADJUNCTIVE UPSTREAM THERAPY DURING ATRIAL FIBRILLATION – REDO ABLATION PROCEDURES: A Pilot Study,
Role: Investigator,
ReCor Medical, Inc.,
(06/2025 - 06/2026)
Status: Approved
An Evaluation of the Safety and Effectiveness of the Conformal CLAAS System for Left Atrial Appendage Occlusion,
Role: Investigator,
Conformal Medical, Inc.,
(06/2025 - 06/2026)
Status: Approved
Inappropriate Sinus Tachycardia (IST) Registry. A Multicenter Observational Data Registry for Outcomes of Inappropriate SinusTachycardia and Postural Orthostatic Tachycardia Syndrome Treatment,
Role: PI,
AtriCure Inc.,
(12/2024)
Status: Approved
Watchmen FLX™ Left Atrial Appendage Closure Device with Delivery System, or any next generation models approved following study commencement. Placebo,
Role: Investigator,
Hamilton Health Sciences Corporation,
Status: Approved