FDA Pathway to Approval: Clinical Requirements for Renal Denervation - K. J. Cavanaugh, PhD

↳ This is a section part of Moment: CRT 2015 Technology & Innovation - Future Clinical Trial Designs and Regulatory Requirements to Assess Efficacy of Devices for the Treatment of Renal Denervation

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Summary

FDA Pathway to Approval: Clinical Requirements for Renal Denervation presented by K. J. Cavanaugh, PhD at CRT 2015

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Target Audience

  • Interventional Cardiologists
  • Interventional Fellows
  • Physicians

Session Name: Future Clinical Trial Designs and Regulatory Requirements to Assess Efficacy of Devices for the Treatment of Renal Denervation

Track: Technology & Innovation

Learning Objectives

  • Updates in Renal Denervation and Hypertension Therapies

Other Components in this Moment

Overview
Patient Characteristics and Impact of Background Clinical Characteristics and Drug Therapies - Raymond Townsend, MD
Proposed Phase 1 Renal Denervation Trial Design in Stage 2 Hypertension - William B. White, MD
How to Follow Patients with Hypertension: Office vs. Ambulatory - Felix Mahfoud, MD
What are the Risks with the Proposed Second Round of Clinical Trials with RDN? - Ron Waksman, MD
FDA Pathway to Approval: Clinical Requirements for Renal Denervation - K. J. Cavanaugh, PhD
What is the Evidence from Surgical Sympathectomies? - V. Papademetriou, MD, DSc
Academic Requirements for Approval of Renal Denervation: Endpoints for the Studies - John C. Somberg, MD
Clinical Pathways for Renal Denervation Research for the Treatment of Refractory and Moderate Hypertension - Laura Mauri, MD
Separation of Sham and Hawthorne Effects - Paul A. Sobotka, MD
Is Renal Denervation a Viable Therapy for Moderate Hypertension? - Raymond Townsend, MD
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