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Phase II randomized sham-controlled study of renal denervation for individuals with uncontrolled hypertension - WAVE IV
RE. Schmieder, C. Ott, SW. Toennes, P. Bramlage, M. Gertner, O. Dawood, P. Baumgart, B. O'Brien, I. Dasgupta, G. Nickenig, J. Ormiston, M. Saxena, ASP. Sharp, H. Sievert, J. Spinar, Z. Starek, J. Weil, U. Wenzel, A. Witkowski, MD. Lobo,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu klinické zkoušky, fáze II, časopisecké články, randomizované kontrolované studie
- MeSH
- ablace intenzivním ultrazvukovým paprskem * MeSH
- antihypertenziva terapeutické užití MeSH
- denervace * MeSH
- dvojitá slepá metoda MeSH
- hypertenze chirurgie MeSH
- krevní tlak MeSH
- ledviny inervace MeSH
- lidé středního věku MeSH
- lidé MeSH
- měření krevního tlaku MeSH
- neúspěšná terapie MeSH
- předčasné ukončení klinických zkoušek MeSH
- prospektivní studie MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze II MeSH
- randomizované kontrolované studie MeSH
OBJECTIVES: The aim of this double-blind, randomized, sham-controlled study was to verify the blood pressure (BP)-lowering efficacy of externally delivered focused ultrasound for renal denervation (RDN). BACKGROUND: Nonrandomized, first proof-of-concept study and experimental evidence suggested that noninvasive techniques of RDN emerged as an alternative approach of RDN to invasive technologies. METHODS: WAVE IV, an international, randomized (1 : 1) sham-controlled, double-blind prospective clinical study, was prematurely stopped. Patients were enrolled if office BP was at least 160 mmHg and 24-h ambulatory BP was at least 135 mmHg, while taking three or more antihypertensive medications. The treatment consisted of bilateral RDN using therapeutic levels of ultrasound energy and the sham consisted of bilateral application of diagnostic levels of ultrasound energy. RESULTS: In the 81 treated patients neither changes in office BP at 12 and 24 weeks, nor changes in 24-h ambulatory BP at 24-week follow-up visit differed between the two groups significantly. Of note, no safety signal was observed. Adherence analysis disclosed full adherence in 77% at baseline and 82% at 6 months' follow-up visit. Post hoc analysis revealed that stricter criteria for stabilization of BP at baseline were associated with a numerically greater change in 24-h ambulatory BP in the RDN group than in the sham group. CONCLUSION: Our data did not prove that antihypertensive efficacy of the externally delivered focused ultrasound for RDN was greater than the sham effect. Stabilization of BP at baseline was identified as an important determinant of BP changes.
Cardiology Department University Hospital Brno Medical Faculty Masaryk University Brno
CardioVascular Center Sankt Katharinen Hospital Frankfurt Germany
Department of Interventional Cardiology and Angiology Institute of Cardiology Warsaw Poland
Institute for Preventive Medicine Mahlow Germany
Institute of Legal Medicine Forensic Toxicology Department Goethe University Frankfurt Main
Kardiologie Angiologie und Pneumologie Universitätsklinikum Bonn Bonn Germany
Kona Medical Bellevue Washington USA
Kona Medical Department of Surgery Stanford School of Medicine Stanford California
Medizinische Klinik 1 Clemenshospital GmbH Münster Germany
Medizinische Klinik 2 Kardiologie und Angiologie Sana Kliniken Lübeck Lübeck
Mercy Angiography Auckland New Zealand
NIHR Barts Cardiovascular Biomedical Research Unit William Harvey Research Institute
Renal Unit Heart of England NHS Foundation Trust Birmingham UK
Royal Exeter and Devon Hospital Exeter UK
Universitätsklinikum Hamburg Eppendorf 3 Medizinische Klinik und Poliklinik Hamburg Germany
Citace poskytuje Crossref.org
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- $a OBJECTIVES: The aim of this double-blind, randomized, sham-controlled study was to verify the blood pressure (BP)-lowering efficacy of externally delivered focused ultrasound for renal denervation (RDN). BACKGROUND: Nonrandomized, first proof-of-concept study and experimental evidence suggested that noninvasive techniques of RDN emerged as an alternative approach of RDN to invasive technologies. METHODS: WAVE IV, an international, randomized (1 : 1) sham-controlled, double-blind prospective clinical study, was prematurely stopped. Patients were enrolled if office BP was at least 160 mmHg and 24-h ambulatory BP was at least 135 mmHg, while taking three or more antihypertensive medications. The treatment consisted of bilateral RDN using therapeutic levels of ultrasound energy and the sham consisted of bilateral application of diagnostic levels of ultrasound energy. RESULTS: In the 81 treated patients neither changes in office BP at 12 and 24 weeks, nor changes in 24-h ambulatory BP at 24-week follow-up visit differed between the two groups significantly. Of note, no safety signal was observed. Adherence analysis disclosed full adherence in 77% at baseline and 82% at 6 months' follow-up visit. Post hoc analysis revealed that stricter criteria for stabilization of BP at baseline were associated with a numerically greater change in 24-h ambulatory BP in the RDN group than in the sham group. CONCLUSION: Our data did not prove that antihypertensive efficacy of the externally delivered focused ultrasound for RDN was greater than the sham effect. Stabilization of BP at baseline was identified as an important determinant of BP changes.
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