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
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hippocratio General Hospital Coordinator of this site? Confirm its status | Athens | Greece | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.