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Comparison Between a Robotic Tele-echo-cardiography Technique and a Standard Echocardiogra

The TERdeblue-S study is a feasibility study of robotic remote echocardiography, not only in terms of technology but also in terms of its integration into a telemedicine system to improve access to the heart failure management system in the Guadeloupe archipelago. The main objective of this study is to study the agreem

Condition(s)Heart Failure, Remote Consultation, Teleconsultation, Echocardiography, Doppler
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThe TERdeblue-S study is a feasibility study of robotic remote echocardiography, not only in terms of technology but also in terms of its integration into a telemedicine system to improve access to the heart failure management system in the Guadeloupe archipelago. The main objective of this study is to study the agreement of the measurement of the left ventricular ejection fraction (FejVG) between in situ echocardiography (EIS) and two-dimensional remote echocardiography (TER) (distance and volumes).
Who can participateInclusion Criteria: * Age ≥18 years * Free, informed and written consent signed by the participant and the investigator * Person affiliated or benefiting from a social security scheme. * Patient meeting at least one of the following criteria: * Systematic cardiovascular check-up or asymptomatic patient with cardiovascular risk factor (hypertension, diabetes, obesity, tobacco, alcohol) * Clinical suspicion of heart disease and/or chronic heart failure with stability of at least one week. * Family history of heart disease and/or sudden death Exclusion Criteria: * Patient requiring urgent cardiological management with transfer to the University Hospital * Acute unstable heart failure, admission to CH Marie-Galante less than 5 days (less than one week) * Pregnant women
Ages18 Years
SexAll
Lead sponsorCentre Hospitalier Universitaire de la Guadeloupe
LocationsGrand-Bourg, Guadeloupe; Petit-Bourg, Guadeloupe; Petit-Canal, Guadeloupe
Start date2025-11-30
NCT IDNCT07265986
Official listinghttps://clinicaltrials.gov/study/NCT07265986

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