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NCT Number: NCT06278844

Exercise Capacity Improvement by Conduction System Pacing in heArt Failure patieNts Without Compelling CRT inDication

This randomized controlled trial aims to investigate the impact of conduction system pacing in comparison to right ventricular apical pacing on exercise capacity, as measured by peak oxygen uptake (VO2peak), in heart failure patients with indication for pacing but no compelling indication for cardiac resynchronization therapy (CRT). The mechanisms of exercise intolerance in heart failure patients influenced by conduction system pacing will be assessed.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Universitair Ziekenhuis Antwerpen

Edegem, Antwerp, 2650, Belgium

Location status: Recruiting

Location contact

Faro Verelst

CONTACT

[email protected]

038213538

About this study

Heart failure (HF) is a serious condition that affects a lot of people and places a significant burden on the healthcare system. Some HF patients also have issues with the natural electrical system of their heart, causing uneven heart contractions and worsening heart function. A treatment known as CRT has been helping such patients, but it does not work for everyone. A new technique called conduction system pacing (CSP) has emerged that might offer a more natural way of maintaining heart contractions.

This study aims to determine if CSP can enhance the ability of HF patients to exercise, by looking at their maximum oxygen consumption (a measure of exercise capacity). It will also explore why some HF patients struggle with exercise more than others. Eligible patients will be randomly assigned to either the new CSP treatment or a standard pacing method (right ventricular apical pacing). Patients will be checked regularly over a follow-up period of 24 weeks.

The main goal is to see if patients can exercise better with CSP after 24 weeks. The study will also look at other heart measures and safety concerns related to the devices. This study might show that CSP can help improve exercise capacity and heart function in certain HF patients. The results could guide health care professionals in offering better, tailored treatments for their patients.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Patients with heart failure as defined by European Society of Cardiology guidelines

  • Signs and/or symptoms of heart failure
  • AND LVEF <50% OR LVEF ≥50% and objective evidence of cardiac structural and/or functional abnormalities consistent with the presence of LV diastolic dysfunction/raised filling pressures
  • AND indication for cardiac pacing as defined by European Society of Cardiology guidelines

Exclusion criteria

  • Age under 18 years old
  • Pregnancy
  • Inability to provide consent or to undergo follow-up
  • Class 1A indication for classical CRT as defined by European Society of Cardiology guidelines. Patients with a class 2A or higher indication for CRT can be included. However, patients with Class 1A indication for classical CRT but failure or suboptimal result of CS lead placement can be included.
  • Significant cardiac or extracardiac comorbidity precluding maximal exercise testing, examples: Recent (<4 weeks) decompensation of heart failure, angina pectoris class ≥2 , uncontrolled hypertension or arrhythmia , severe valvular heart disease, significant peripheral vascular disease, orthopaedic limitation ...
  • Comorbidity that may influence 6-month prognosis, examples:

Severe chronic kidney disease (eGFR ≤20 mL/kg/min or dialysis) , severe chronic obstructive pulmonary disease (≥GOLD 3) , active malignancy ...

Treatment and study plan

conduction system pacing

Device

In the conduction system pacing group, the right ventricular lead will be placed in a septal position to achieve conduction system pacing, either His bundle pacing (HBP) or left bundle branch area (LBBA) pacing. In the usual care group, the right ventricular lead will be placed in the right ventricle apex as usual.

Right ventricular apical pacing

Device

This is the usual care group. Patients will receive a pacemaker device with the right ventricular lead inserted in the apex and not in the septal position.

Primary outcomes

  1. Exercise capacity

    Time frame: 24 weeks after pacemaker implantation

    Change of VO2 peak from baseline to 24 weeks

Secondary outcomes

  1. Exercise capacity

    Time frame: 4 weeks after pacemaker implantation

    Change of VO2 peak from baseline to 4 weeks

  2. Echocardiographic parameters (Ejection Fraction)

    Time frame: 4, 12 and 24 weeks after pacemaker implantation

    Change from baseline to 4,12 and 24 weeks (EF%)

  3. QRS width

    Time frame: 4, 12 and 24 weeks after pacemaker implantation

    Change from baseline to 4,12,24 weeks (msec)

  4. Biomarker, N-terminal pro B-type natriuretic peptide levels

    Time frame: 4 and 24 weeks after pacemaker implantation

    Change from baseline to 4, 24 weeks (pg/ml)

  5. Health-related quality of life scores

    Time frame: 4,12 and 24 weeks after pacemaker implantation

    KCCQS - Kansas City cardiomyopathy quality score

Study contacts

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

Andreas Gevaert

CONTACT

[email protected]

038213538

Faro Verelst

CONTACT

[email protected]

038213538

Sponsors and collaborators

Lead sponsor

University Hospital, Antwerp

Other

Registry information

Acronym: ESCPAND

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
Feb 26, 2024
Registry last updated
Feb 26, 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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