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NCT Number: NCT05715697

Renal Denervation in Patients With Chronic Heart Failure With Preserved Ejection Fraction

This study aims to explore the potential of RDN as a therapy for HFpEF in a Prospective, Multicenter, Randomized, Blinded, Sham-controlled Study.

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Key information

Age range

21 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Heart failure is one of the most important diseases worldwide, with a 5-year mortality of up to 75% in symptomatic patients. While substantial progress has been made in the treatment of patients with reduced left ventricular ejection fraction (HFrEF), mortality for patients with heart failure and preserved ejection fraction (HFpEF) remains unchanged, despite a comparable prevalence and mortality of the disease as for heart failure with reduced ejection fraction. Heart failure with preserved ejection fraction has a high mortality, which is contrasted by a total absence of therapy options besides symptomatic diuretic treatment. This study aims to explore the potential of RDN as a therapy for HFpEF in a Prospective, Multicenter, Randomized, Blinded, Sham-controlled Study.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • signs or symptoms of heart failure;
  • normal or mildly abnormal systolic LV function (LVEF ≥ 50%);
  • evidence of diastolic LV dysfunction.
  • Individual should fulfill the diagnostic WHO criteria for hypertension: SBP > 140 mmHg and/or DBP > 90 mmHg, and is treated with at least 2 antihypertensive drugs. This treatment is expected to be maintained for at least 6 months. Using this regimen the blood pressure should be adequately controlled (< 140/90mmHg by 24 hour ambulatory BP measurement).
  • Individual is adhering to a stable drug regimen HFNEF, with no changes for a minimum of 2 weeks prior to enrollment, and which is expected to be maintained for at least 6 months.

Exclusion criteria

  • Known secondary cause of hypertension
  • Anatomy not eligible for renal denervation
  • Systolic heart failure (LVEF < 50%)
  • Individual has an estimated glomerular filtration rate (eGFR) of < 30mL/min/1.73m2, using the MDRD calculation.
  • Individual has any serious medical condition, which in the opinion of the investigator, may adversely affect the safety and/or effectiveness of the participant or the study (i.e., patients with clinically significant peripheral vascular disease, abdominal aortic aneurysm, bleeding disorders such as thrombocytopenia, haemophilia, significant anaemia, or arrhythmias such as atrial fibrillation).
  • Individual is pregnant, nursing or planning to be pregnant.

Treatment and study plan

Sham procedure and maintenance of heart failure medications

Procedure

Sham intervention, maintenance of heart failure medications

Renal denervation and maintenance of heart failure medications

Procedure

Renal denervation and maintenance of heart failure medications

Primary outcomes

  1. Change from baseline E/E' at 12 months

    Time frame: 12 months after treatment

    Echocardiography will be used to measure the E/E'

Secondary outcomes

  1. Number of participants with adverse events

    Time frame: 1 year

Study contacts

Contact information is provided by the study sponsor or research team.

Xiang Xie

CONTACT

[email protected]

+869914366892

Sponsors and collaborators

Lead sponsor

Xinjiang Medical University

Other

Collaborators

  • First Affiliated Hospital of Xinjiang Medical University

Registry information

Official study title

The First Affiliated Hospital of Xinjiang Medical University

Acronym: RDN-HFPEF

Important dates

Study start
2023
Primary completion
2024
Study completion
2026
First posted
Feb 8, 2023
Registry last updated
Feb 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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