Universitair Ziekenhuis Antwerpen
Edegem, Antwerp, 2650, Belgium
Location status: Recruiting
NCT Number: NCT06278844
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Edegem, Antwerp, 2650, Belgium
Location status: Recruiting
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.
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
Exclusion criteria
Severe chronic kidney disease (eGFR ≤20 mL/kg/min or dialysis) , severe chronic obstructive pulmonary disease (≥GOLD 3) , active malignancy ...
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.
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.
Time frame: 24 weeks after pacemaker implantation
Change of VO2 peak from baseline to 24 weeks
Time frame: 4 weeks after pacemaker implantation
Change of VO2 peak from baseline to 4 weeks
Time frame: 4, 12 and 24 weeks after pacemaker implantation
Change from baseline to 4,12 and 24 weeks (EF%)
Time frame: 4, 12 and 24 weeks after pacemaker implantation
Change from baseline to 4,12,24 weeks (msec)
Time frame: 4 and 24 weeks after pacemaker implantation
Change from baseline to 4, 24 weeks (pg/ml)
Time frame: 4,12 and 24 weeks after pacemaker implantation
KCCQS - Kansas City cardiomyopathy quality score
Contact information is provided by the study sponsor or research team.
Andreas Gevaert
CONTACT
Faro Verelst
CONTACT
University Hospital, Antwerp
Other
Acronym: ESCPAND
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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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