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NCT07742787Active, not recruiting

Renal Denervation in Chronic Kidney Disease - RDN-CKD Study

Effect of Renal Denervation on Blood Pressure in Patients With Chronic Kidney Disease and Uncontrolled Hypertension

Source: ClinicalTrials.gov · Last updated 4 Aug 2026

Brief summary (registry, in English)

RDN-CKD GR Study is a prospective, randomized (1:1), double-blind (unblinded interventionalist and blinded study team), sham controlled study. The purpose of the RDN-CKD GR Study is to demonstrate that renal denervation (RDN) effectively reduces 24-h ambulatory BP in 20 patients with chronic kidney disease (CKD) stage 3a or 3b.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
20 (actual)
First submitted
29 Jul 2026
Start date
4 Jul 2024
Primary completion date
6 Sept 2026
Lead sponsor
Hippocration General Hospital
NCT number
NCT07742787

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From 4 Jul 2024 to the primary completion date, 6 Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior renal denervation procedure
  • Anatomic or functional solitary kidney, kidney transplantation

Other illness

  • Other cause of Hypertension that can be treated by Intervention/surgery (e.g. hemodynamically relevant renal artery stenosis, functional adrenal adenoma)
  • Secondary hypertension other than obstructive sleep apnea
  • Type 1 diabetes mellitus
  • Nephrotic syndrome
  • Individual has experienced a myocardial infarction, unstable angina pectoris, or a cerebrovascular accident within 3 months of the screening visit
  • Acute episode of renal disease requiring uptitration of any immunosuppressive drug regimen within the last 3 months
  • Any condition that, at the discretion of the investigator, would preclude participation in the study (e.g. non-adherence)

Lab values

  • Lack of capturing serum creatinine levels in the past

Other

  • Anatomically significant renal artery abnormality in either renal artery which in the eyes of the interventionalist would interfere with safe catheter Placement
  • Office (attended) BP ≥ 180 mmHg systolic and/or ≥ 110 mmHg diastolic
  • 24-h ambulatory BP ≥ 160 mmHg systolic
  • Contraindication to magnetic resonance imaging (MRI)
  • Subject is pregnant, nursing, or intends to become pregnant
  • Enrollment in another interventional research protocol.

Who the study is looking for

  • CKD stage 3 (eGFR 30-59 ml/min/1.73m² \[according to the currently used estimation formulas: MDRD, CKD-EPI\]) with diabetic or non-diabetic nephropathy
  • Uncontrolled hypertension with 1-5 drug classes (renin angiotensin system \[RAS\] blockade is mandatory, unless intolerance to RAS blockers has been documented) and systolic office (attended) BP ≥140 mmHg confirmed by 24-h ambulatory BP systolic ≥130 mmHg
  • Patient is adhering to a stable drug regimen including RAS blockade without changes for a minimum of 4 weeks.
  • Individual is ≥ 18 years of age, both genders are included

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hippocratio General Hospital
Coordinator of this site? Confirm its status
AthensGreeceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.