Prediction of Blood Pressure Outcomes Following Renal Denervation (PREDICT-RDN)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHeart Center Leipzig - University Hospital

About this trial

Prospective, single arm trial to assess the effects of renal denervation on day-by-day blood pressure measurements and time in blood pressure target range, as well as establish a multivariate prediction model for blood pressure reduction after renal denervation.

Eligibility criteria

Qualifiers

Confirmed arterial hypertension with systolic or diastolic blood pressure >140/90 mmHg in standardized office blood pressure measurement

Treatment with 3 to ≤5 antihypertensive drug classes

Age >18 years

Written informed consent

Disqualifiers

Age ≤ 18 years

anatomy unsuitable for renal denervation (i.e. renal artery stenosis, single functioning kidney)

pregnancy

patients under legal supervision or guardianship

Trial design

Treatments tested in this trial

  • Renal sympathetic denervation

Treatment groups

90 Participants
are divided into 1 treatment group

Sponsors and collaborators

Heart Center Leipzig - University Hospital

Lead sponsor

Helios Health Institute GmbH

Collaborator