SELUTION SLR™ 014 ISR: A Prospective Randomized Single Blind Multicenter Study to Assess the Safety and Effectiveness of the SELUTION SLR™ 014 Drug Eluting Balloon in the Treatment of Subjects with In-stent Restenosis,
Role: Investigator,
MedAlliance,
(06/2024 - 06/2025)
Status: Approved
SSO2 THERAPY: AMIHOT III STUDY: A MULTI-CENTER RANDOMIZED POST-APPROVAL EVALUATION OF THE DELIVERY OF INTRACORONARY HYPEROXEMIC SUPERSATURATED OXYGEN THERAPY FOR 60 MINUTES IN ANTERIOR ACUTE MYOCARDIAL INFARCTION PATIENTS WITH SUCCESSFUL REPERFUSION (VIA PCI) = SIX HOURS AFTER SYMPTOM ONSET COMPARED TO STANDARD THERAPY,
Role: Investigator,
TherOx, Inc.,
(05/2024 - 05/2025)
Status: Approved
Ultrasound-based renal sympathetic denervation as adjunctive upstream therapy during atrial fibrillation ablation: a pilot study (ULTRA-HFIB),
Role: Investigator,
ReCor Medical, Inc.,
(01/2025 - 01/2026)
Status: Approved