TY - JOUR
T1 - Endovascular ultrasound renal denervation to treat hypertension (RADIANCE-HTN SOLO)
T2 - a multicentre, international, single-blind, randomised, sham-controlled trial
AU - Azizi, Michel
AU - Schmieder, Roland E
AU - Mahfoud, Felix
AU - Weber, Michael A
AU - Daemen, Joost
AU - Davies, Justin
AU - Basile, Jan
AU - Kirtane, Ajay J
AU - Wang, Yale
AU - Lobo, Melvin D
AU - Saxena, Manish
AU - Feyz, Lida
AU - Rader, Florian
AU - Lurz, Philipp
AU - Sayer, Jeremy
AU - Sapoval, Marc
AU - Levy, Terry
AU - Sanghvi, Kintur
AU - Abraham, Josephine
AU - Sharp, Andrew S P
AU - Fisher, Naomi D L
AU - Bloch, Michael J
AU - Reeve-Stoffer, Helen
AU - Coleman, Leslie
AU - Mullin, Christopher
AU - Mauri, Laura
AU - Voskuil, Michiel
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/6/9
Y1 - 2018/6/9
N2 - BACKGROUND: Early studies suggest that radiofrequency-based renal denervation reduces blood pressure in patients with moderate hypertension. We investigated whether an alternative technology using endovascular ultrasound renal denervation reduces ambulatory blood pressure in patients with hypertension in the absence of antihypertensive medications.METHODS: RADIANCE-HTN SOLO was a multicentre, international, single-blind, randomised, sham-controlled trial done at 21 centres in the USA and 18 in Europe. Patients with combined systolic-diastolic hypertension aged 18-75 years were eligible if they had ambulatory blood pressure greater than or equal to 135/85 mm Hg and less than 170/105 mm Hg after a 4-week discontinuation of up to two antihypertensive medications and had suitable renal artery anatomy. Patients were randomised (1:1) to undergo renal denervation with the Paradise system (ReCor Medical, Palo Alto, CA, USA) or a sham procedure consisting of renal angiography only. The randomisation sequence was computer generated and stratified by centres with randomised blocks of four or six and permutation of treatments within each block. Patients and outcome assessors were blinded to randomisation. The primary effectiveness endpoint was the change in daytime ambulatory systolic blood pressure at 2 months in the intention-to-treat population. Patients were to remain off antihypertensive medications throughout the 2 months of follow-up unless specified blood pressure criteria were exceeded. Major adverse events included all-cause mortality, renal failure, an embolic event with end-organ damage, renal artery or other major vascular complications requiring intervention, or admission to hospital for hypertensive crisis within 30 days and new renal artery stenosis within 6 months. This study is registered with ClinicalTrials.gov, number NCT02649426.FINDINGS: Between March 28, 2016, and Dec 28, 2017, 803 patients were screened for eligibility and 146 were randomised to undergo renal denervation (n=74) or a sham procedure (n=72). The reduction in daytime ambulatory systolic blood pressure was greater with renal denervation (-8·5 mm Hg, SD 9·3) than with the sham procedure (-2·2 mm Hg, SD 10·0; baseline-adjusted difference between groups: -6·3 mm Hg, 95% CI -9·4 to -3·1, p=0·0001). No major adverse events were reported in either group.INTERPRETATION: Compared with a sham procedure, endovascular ultrasound renal denervation reduced ambulatory blood pressure at 2 months in patients with combined systolic-diastolic hypertension in the absence of medications.FUNDING: ReCor Medical.
AB - BACKGROUND: Early studies suggest that radiofrequency-based renal denervation reduces blood pressure in patients with moderate hypertension. We investigated whether an alternative technology using endovascular ultrasound renal denervation reduces ambulatory blood pressure in patients with hypertension in the absence of antihypertensive medications.METHODS: RADIANCE-HTN SOLO was a multicentre, international, single-blind, randomised, sham-controlled trial done at 21 centres in the USA and 18 in Europe. Patients with combined systolic-diastolic hypertension aged 18-75 years were eligible if they had ambulatory blood pressure greater than or equal to 135/85 mm Hg and less than 170/105 mm Hg after a 4-week discontinuation of up to two antihypertensive medications and had suitable renal artery anatomy. Patients were randomised (1:1) to undergo renal denervation with the Paradise system (ReCor Medical, Palo Alto, CA, USA) or a sham procedure consisting of renal angiography only. The randomisation sequence was computer generated and stratified by centres with randomised blocks of four or six and permutation of treatments within each block. Patients and outcome assessors were blinded to randomisation. The primary effectiveness endpoint was the change in daytime ambulatory systolic blood pressure at 2 months in the intention-to-treat population. Patients were to remain off antihypertensive medications throughout the 2 months of follow-up unless specified blood pressure criteria were exceeded. Major adverse events included all-cause mortality, renal failure, an embolic event with end-organ damage, renal artery or other major vascular complications requiring intervention, or admission to hospital for hypertensive crisis within 30 days and new renal artery stenosis within 6 months. This study is registered with ClinicalTrials.gov, number NCT02649426.FINDINGS: Between March 28, 2016, and Dec 28, 2017, 803 patients were screened for eligibility and 146 were randomised to undergo renal denervation (n=74) or a sham procedure (n=72). The reduction in daytime ambulatory systolic blood pressure was greater with renal denervation (-8·5 mm Hg, SD 9·3) than with the sham procedure (-2·2 mm Hg, SD 10·0; baseline-adjusted difference between groups: -6·3 mm Hg, 95% CI -9·4 to -3·1, p=0·0001). No major adverse events were reported in either group.INTERPRETATION: Compared with a sham procedure, endovascular ultrasound renal denervation reduced ambulatory blood pressure at 2 months in patients with combined systolic-diastolic hypertension in the absence of medications.FUNDING: ReCor Medical.
KW - Adolescent
KW - Adult
KW - Aged
KW - Blood Pressure Monitoring, Ambulatory/trends
KW - Denervation/methods
KW - Endovascular Procedures/methods
KW - Female
KW - Humans
KW - Hypertension/surgery
KW - Kidney/blood supply
KW - Male
KW - Middle Aged
KW - Renal Artery/innervation
KW - Single-Blind Method
KW - Treatment Outcome
KW - Ultrasonography/instrumentation
KW - Young Adult
U2 - 10.1016/S0140-6736(18)31082-1
DO - 10.1016/S0140-6736(18)31082-1
M3 - Article
C2 - 29803590
SN - 0140-6736
VL - 391
SP - 2335
EP - 2345
JO - The Lancet
JF - The Lancet
IS - 10137
ER -