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NCT07893821Recruiting

Renal Denervation in Patients With Atrial Fibrillation and Hypertension

A Pilot Study Evaluating Renal Denervation in Heart Failure Patients: A Two-Phase Prospective Study - Phase 1

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

High blood pressure is a major risk factor for atrial fibrillation (AF), an irregular heart rhythm, and heart failure with preserved ejection fraction (HFpEF), a condition in which the heart becomes stiff and cannot relax properly. Both conditions can significantly affect quality of life and frequently occur together. In individuals with high blood pressure, increased activity of the nerves surrounding the kidneys can further elevate blood pressure and contribute to strain on the heart. Renal denervation (RDN) is a procedure designed to lower blood pressure by reducing the activity of these nerves using a thin catheter and controlled energy. RDN has been shown to lower blood pressure safely in many patients; however, the potential benefits in individuals with concurrent AF and HFpEF remain uncertain. This pilot study will be conducted in two phases. Phase 1 will assess the safety and feasibility of accessing the renal arteries and evaluating blood pressure responses to brief electrical stimulation of the renal nerves.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
18 Sept 2026
Start date
1 Aug 2026
Primary completion date
Aug 2029
Lead sponsor
Pavel Antiperovitch
NCT number
NCT07893821

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 1 Aug 2026 to the primary completion date, Aug 2029
  • 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

  • Previous renal artery intervention

Other

  • Hemodynamic instability
  • Renal artery stenosis \>50%
  • Single functioning kidney
  • Pregnancy or nursing
  • Life expectancy \<12 months
  • Unwilling or unable to provide informed consent
  • Participation in a clinical trial that may impact the outcomes of the current study

Who the study is looking for

  • Age ≥18 years
  • Scheduled for EP study +/- catheter ablation
  • Adequate renal function (eGFR ≥45 mL/min/1.73m²)

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
London Heart Rhythm Program
Coordinator of this site? Confirm its status
LondonCanadaRecruiting

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