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Study design: Investigator initiated, single centre, feasibility study
Main objectives are twofold:
Study population: 40 patients (18 - 80 yr old)
Full description
Background: Approximately 10-15% of adults with hypertension are considered to be treatment resistant because their hypertension is uncontrolled despite taking three or more drugs that includes a diuretic. Renal denervation (RDN) is a novel treatment option for therapy resistant hypertension and its rationale originates in denervating the renal sympathetic efferent and afferent coupling with the central autonomic nervous system. By denervating the renal arteries, general sympathetic tone is reduced. Currently, RDN is performed by placing in a spiral pattern 5-6 ablation lesions in each renal artery. 15-30% of the patients do not have any benefit from this procedure. The reason for this is unknown. Experimental data show that renal nerve stimulation (RNS) may serve as a functional endpoint to assess completeness of the RDN procedure. A RNS-guided RDN may prove to be superior to standard RDN (RNS-checked) in blood pressure control.
Main objectives are twofold:
Secondary objective:
The secondary objective is to compare both techniques (RNS-checked vs. RNS-guided) in terms of efficacy and safety.
Hypotheses:
Study design: Investigator initiated, single centre, prospective, feasibility study
Study population: 40 patients (18 - 80 yr old)
Intervention:
Two different techniques will be used in this trial:
Main study endpoints:
Main study parameter will be the arterial blood pressure response to RNS prior to RDN and absence of blood pressure rise in response to pacing in the renal artery after RDN.
Secondary study endpoints:
Blood pressure at 3, 6, 12 months after the intervention, and change in blood pressure compared to measurement before the intervention.
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56 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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