Global registry aims to improve heart pacing for rhythm disorders
NCT ID NCT04831125
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study gathered information from 383 people with slow heartbeats or heart failure who received a special type of pacemaker called conduction system pacing. Researchers looked at how well the device worked, any complications, and changes in heart function over 12 months. The goal was to learn more about the strengths and limits of this pacing method to guide future treatments.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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383 people
The number who actually took part.
- Started
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Apr 2021
- Finished
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Feb 2026
- 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.
Who is studied
Individuals receiving conduction system pacing * Any presence of symptomatic bradyarrhythmia requiring pacing therapy * Any presence of heart failure (HF) with evidence of wide QRS or anticipated requirement for \>40% ventricular pacing
- Ages
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18 years and older
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Meets American College of Cardiology (ACC)/American Heart Association (AHA)/Heart Rhythm Society (HRS) guidelines for bradycardia, or * Meets ACC/AHA/HRS guidelines for cardiac resynchronization therapy (CRT). Exclusion Criteria: * Age \< 18 years * Inability of patient capacity to provide consent for themselves either due to medical or psychiatric comorbidity * Pregnancy * Difficulty with follow-up
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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.
Contacts and locations
Locations
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Geisinger Wyoming Valley Medical Center
Wilkes-Barre, Pennsylvania, 18711, United States
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Health Research Institute Hospital La Fe
Valencia, Spain
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Icahn School of Medicine at Mount Sinai & Mount Sinai Hospital
New York, New York, 10029, United States
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Lund University
Lund, Sweden
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Maastricht University Medical Center
Maastricht, Netherlands
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University of Arizona
Tucson, Arizona, 85719, United States
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University of Chicago
Chicago, Illinois, 60637, United States
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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
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