Actively Recruiting
Prediction of Blood Pressure Outcomes Following Renal Denervation (PREDICT-RDN)
Led by Heart Center Leipzig - University Hospital · Updated on 2025-06-24
90
Participants Needed
2
Research Sites
143 weeks
Total Duration
On this page
Sponsors
H
Heart Center Leipzig - University Hospital
Lead Sponsor
H
Helios Health Institute GmbH
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Prediction of Blood Pressure Outcomes Following Renal Denervation (PREDICT-RDN)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Confirmed arterial hypertension with systolic or diastolic blood pressure >140/90 mmHg in standardized office blood pressure measurement
- Treatment with 3 to 45 antihypertensive drug classes
- Age >18 years
- Written informed consent
You will not qualify if you...
- Age 4 18 years
- Anatomy unsuitable for renal denervation (i.e. renal artery stenosis, single functioning kidney)
- Pregnancy
- Patients under legal supervision or guardianship
- Participation in other trials that might interfere with the study outcome according to the opinion of one of the investigators
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Universitätsmedizin Mainz Kardiologie I
Mainz, Rheinland Pflanz, Germany, 55131
Not Yet Recruiting
2
Heart Center Leipzig
Leipzig, Saxony, Germany, 04289
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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