Heart mapping study aims to understand electrical vs. mechanical timing in fallot patients
NCT ID NCT05485545
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study was designed to compare electrical and mechanical activation of the right ventricle in adults who had surgery for Tetralogy of Fallot, a congenital heart condition. Researchers planned to use 3D mapping and imaging to see if electrical signals match the heart's physical movement. However, the study was withdrawn before enrolling any participants, so no results are available.
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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.
- Expected to start
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Sep 2022
An estimate. Start dates often move.
- Expected to finish
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Sep 2024
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 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.
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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: Inclusion Criteria in the Fallot group * Male or female patient aged 18, * Patient with Fallot Tetralogy operated. nclusion Criteria in the Control group * Male or female patient aged 18, * Patient benefiting from electrophysiological exploration for a healthy heart arrhythmia, * Patient with a significant lack of heart disease. Exclusion Criteria: Exclusion Criteria in the Fallot group * Patient with associated left heart disease, * Patient with an acoustic window that does not allow for proper echocardiography, * Patient with contraindication to MRI, * Woman of childbearing age without effective contraception (HAS criteria) or Pregnant (ßHCG \> 20 IU/l) or nursing woman. Exclusion Criteria in the Control group * Patient with an acoustic window that does not allow proper echocardiography, * Patient with MRI contraindication, * Woman of childbearing age without effective contraception (HAS criteria) or Pregnant (ßHCG \> 20 IU/l) or nursing woman, * Cardiac pathology detected during echocardiography.
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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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CHU de Bordeaux
Bordeaux, France
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Other studies related to the condition(s) this trial covers.
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