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A Post-Approval, Single-Arm Study of the SYNERGY Stent System in China

A prospective, observational, single-arm, open-label, multicenter, post-approval study. To compile real-world clinical outcomes data for the SYNERGYTM MONORAILTM Everolimus-Eluting ...

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DENEX, Renal Denervation Therapy, in Patients With Hypertension on no or 1-3 Ant...

The objective of this study is to show that the safety and efficacy of renal denervation using DENEX, are superior...

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NAN-101 in Patients With Class III Heart Failure

This is a Phase 1, prospective, multi-center, open-label, sequential dose escalation study to explore the safety, feasibility, and efficacy of...

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A Study Evaluating the Efficacy and Safety of Ralinepag to Improve Treatment Out...

Study ROR-PH-301, ADVANCE OUTCOMES, is designed to assess the efficacy and safety of ralinepag when added to pulmonary arterial hypertension...

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A Study of Ralinepag to Evaluate Effects on Exercise Capacity by CPET in Subject...

Study ROR-PH-302, ADVANCE CAPACITY, is designed to evaluate the effects of ralinepag therapy on exercise capacity as assessed by change...

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DENEX Renal Denervation in Patients With Hypertension on no Antihypertensive Med...

The objective of this study is to evaluate the safety and effectiveness of renal denervation using DENEX System in patients...