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Published in: Clinical Research in Cardiology 3/2020

Open Access 01-03-2020 | Neurotomy | Trial Design

Rationale and design of two randomized sham-controlled trials of catheter-based renal denervation in subjects with uncontrolled hypertension in the absence (SPYRAL HTN-OFF MED Pivotal) and presence (SPYRAL HTN-ON MED Expansion) of antihypertensive medications: a novel approach using Bayesian design

Authors: Michael Böhm, Raymond R. Townsend, Kazuomi Kario, David Kandzari, Felix Mahfoud, Michael A. Weber, Roland E. Schmieder, Konstantinos Tsioufis, Graeme L. Hickey, Martin Fahy, Vanessa DeBruin, Sandeep Brar, Stuart Pocock

Published in: Clinical Research in Cardiology | Issue 3/2020

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Abstract

Background

The SPYRAL HTN clinical trial program was initiated with two 80-patient pilot studies, SPYRAL HTN-OFF MED and SPYRAL HTN-ON MED, which provided biological proof of principle that renal denervation has a blood pressure-lowering effect versus sham controls for subjects with uncontrolled hypertension in the absence or presence of antihypertensive medications, respectively.

Trial design

Two multicenter, prospective, randomized, sham-controlled trials have been designed to evaluate the safety and efficacy of catheter-based renal denervation for the reduction of blood pressure in subjects with hypertension in the absence (SPYRAL HTN-OFF MED Pivotal) or presence (SPYRAL HTN-ON MED Expansion) of antihypertensive medications. The primary efficacy endpoint is baseline-adjusted change from baseline in 24-h ambulatory systolic blood pressure. The primary safety endpoint is incidence of major adverse events at 1 month after randomization (or 6 months in cases of new renal artery stenosis). Both trials utilize a Bayesian design to allow for prespecified interim analyses to take place, and thus, the final sample sizes are dependent on whether enrollment is stopped at the first or second interim analysis. SPYRAL HTN-OFF MED Pivotal will enroll up to 300 subjects and SPYRAL HTN-ON MED Expansion will enroll up to 221 subjects. A novel Bayesian power prior approach will leverage historical information from the pilot studies, with a degree of discounting determined by the level of agreement with data from the prospectively powered studies.

Conclusions

The Bayesian paradigm represents a novel and promising approach in device-based hypertension trials.

Clinical trial registration

URL: https://​www.​clinicaltrials.​gov. Unique identifier: NCT02439749 (SPYRAL HTN-OFF MED Pivotal) and NCT02439775 (SPYRAL HTN-ON MED Expansion).
Appendix
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Metadata
Title
Rationale and design of two randomized sham-controlled trials of catheter-based renal denervation in subjects with uncontrolled hypertension in the absence (SPYRAL HTN-OFF MED Pivotal) and presence (SPYRAL HTN-ON MED Expansion) of antihypertensive medications: a novel approach using Bayesian design
Authors
Michael Böhm
Raymond R. Townsend
Kazuomi Kario
David Kandzari
Felix Mahfoud
Michael A. Weber
Roland E. Schmieder
Konstantinos Tsioufis
Graeme L. Hickey
Martin Fahy
Vanessa DeBruin
Sandeep Brar
Stuart Pocock
Publication date
01-03-2020
Publisher
Springer Berlin Heidelberg
Published in
Clinical Research in Cardiology / Issue 3/2020
Print ISSN: 1861-0684
Electronic ISSN: 1861-0692
DOI
https://doi.org/10.1007/s00392-020-01595-z

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