Remote tuning for heart devices: no clinic visit needed?
NCT ID NCT05366660
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether doctors can safely check and adjust pacemakers and defibrillators from a remote location, instead of requiring patients to come into the clinic. 110 adults with these heart devices took part. The goal was to see if remote programming works as well as in-person visits, which could save patients time and reduce the need for travel.
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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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110 people
The number who actually took part.
- Started
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Jun 2021
- Finished
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Apr 2022
- 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 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: * Patient of both sexes over the age of 18 * Patients implanted with a cardiac pacemaker or an automatic defibrillator and an indication for device check-up (interrogation ± programming) which may be periodic as part of their follow-up, postoperative, following a remote monitoring alert, pre/post MRI or following symptoms. * Person beneficiary of social security insurance. * Informed consent confirmed in writing (at the latest on the day of inclusion and before any examination required by the research). * Women of procreating age with effective contraception Exclusion Criteria: * Patients younger than 18 years old * Patients who are incapable to understand the study design or to give informed consent. * Pregnant or breastfeeding women * Persons placed under judicial protection, curatorship, tutorship. * Subject deprived of liberty on judicial or administrative decision * Persons participating in another study who are still in their period of exclusion
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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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Bordeaux University Hospital
Pessac, France, 33604, France
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