New heart pacing method may improve life for AF patients with heart failure
NCT ID NCT06152406
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares a new pacing technique (His bundle pacing) to standard right ventricular pacing in 100 adults with symptomatic atrial fibrillation and heart failure who are having AV node ablation. The goal is to see if the new method helps them walk farther, feel better, and be more active. Participants will wear a Fitbit to track daily steps and distance.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2023
- Expected to finish
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Feb 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 18 or above * Symptomatic AF, New York Heart Association (NYHA) class II-IV * Willing to consent for the study * AF regardless type, deemed not suitable for rhythm control strategy that has been referred for AVN ablation with one of the following: 1. Impaired LV function, EF \<50 %. And or 2. Raised N-Terminal Pro B-type Natriuretic Peptide ( NT-ProBNP) \>365 ng/L Exclusion Criteria: * Patient who has already got a pacemaker in situ * Known severe LVSD when biventricular device is the thought to be the preferred pacing modality * Females in child bearing period * Lack of capacity to consent * Other serious medical condition with life expectancy of less than 1 year * Less than 18 years * Unwilling to consent for the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospitals of Leicester NHS Trust
RECRUITINGLeicester, Leicestershire, LE1 5WW, United Kingdom
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Other studies related to the condition(s) this trial covers.
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