[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100634829":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":32,"locations":38,"responsibleParty":206,"collaborators":31,"id":208,"slug":209,"hasResults":210,"nctId":211,"briefTitle":212,"officialTitle":213,"acronym":214,"eligibilityCriteria":215,"healthyVolunteers":210,"sex":216,"minAge":217,"maxAge":31,"enrollmentInfo":218,"targetDuration":31,"studyType":221,"phases":222,"briefSummary":224,"conditions":225,"keywords":227,"overallStatus":152,"whyStopped":31,"lastUpdateSubmitDate":233,"lastUpdatePostDateStruct":234,"startDateStruct":237,"completionDateStruct":239,"leadSponsor":241,"locationsCount":242},{"fullName":5,"class":6},"Poitiers University Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Remote HF management guided with the HeartLogic™ algorithm.","EXPERIMENTAL","After enrolment, patients of the intervention arm will be remotely followed up based on an alert-driven strategy by the local research coordinator. In case of index value ≥16, diuretics should be increased during 4 to 5 days, or HF guidelines directed medication therapy will be up titrated.",[13],"Other: Alert-guided remote follow-up",{"label":15,"type":16,"description":17,"interventionNames":18},"Conventional face-to-face HF management (no monitoring of HeartLogic alerts)","ACTIVE_COMPARATOR","The control group is treated with a usual follow-up. Current guidelines recommend follow-up at intervals no longer than 6 months. They will be monitored at baseline, 6 and 12 months after inclusion.",[19],"Other: Traditional follow up",[21,27],{"type":6,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"Alert-guided remote follow-up","Participants assigned to this intervention will receive alert-guided remote follow-up for heart failure. Device-generated alerts suggestive of worsening heart failure will be reviewed by the study team through the remote monitoring platform. When an alert occurs, patients may be contacted for symptom assessment and clinical evaluation, and treatment may be adjusted preemptively according to a predefined care pathway and local clinical practice.",[9],[26],"HeartLogic-guided remote follow-up",{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"Traditional follow up","Patients will be monitored every 6 months as recommended by the guidelines",[15],null,[33],{"name":34,"role":35,"phone":36,"phoneExt":31,"email":37},"Céline Deletage","CONTACT","+33549443854","celine.deletage@chu-poitiers.fr",[39,54,66,77,88,99,110,122,131,142,150,165,176,187,195],{"facility":40,"status":41,"city":42,"state":31,"zip":31,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"University hospital of Amiens","NOT_YET_RECRUITING","Amiens","France","FR",{"type":46,"coordinates":47},"Point",[48,49],2.3,49.9,{"lat":49,"lon":48},[52],{"name":53,"role":35,"phone":31,"phoneExt":31,"email":31},"Alexis 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Rouen","Rouen",{"type":46,"coordinates":169},[170,171],1.09932,49.44313,{"lat":171,"lon":170},[174],{"name":175,"role":35,"phone":31,"phoneExt":31,"email":31},"Frédéric Anselme",{"facility":177,"status":41,"city":178,"state":31,"zip":31,"country":43,"countryCode":44,"cosmosGeoPoint":179,"geoPoint":183,"contacts":184},"Pasteur clinic","Toulouse",{"type":46,"coordinates":180},[181,182],1.44367,43.60426,{"lat":182,"lon":181},[185],{"name":186,"role":35,"phone":31,"phoneExt":31,"email":31},"Serge Boveda",{"facility":188,"status":41,"city":178,"state":31,"zip":31,"country":43,"countryCode":44,"cosmosGeoPoint":189,"geoPoint":191,"contacts":192},"University hospital of Toulouse",{"type":46,"coordinates":190},[181,182],{"lat":182,"lon":181},[193],{"name":194,"role":35,"phone":31,"phoneExt":31,"email":31},"Romain Itier",{"facility":196,"status":41,"city":197,"state":31,"zip":31,"country":43,"countryCode":44,"cosmosGeoPoint":198,"geoPoint":202,"contacts":203},"University hospital of Tours","Tours",{"type":46,"coordinates":199},[200,201],0.70398,47.39484,{"lat":201,"lon":200},[204],{"name":205,"role":35,"phone":31,"phoneExt":31,"email":31},"Arnaud Bisson",{"type":207,"investigatorFullName":31,"investigatorTitle":31,"investigatorAffiliation":31,"oldNameTitle":31,"oldOrganization":31},"SPONSOR","100634829","heartlogic-in-patients-with-heart-failure-100634829",false,"NCT07544771","HeartLogic™ in Patients With Heart Failure.","HeartLogic™ Evaluation for Remote Monitoring vs. Office-based Follow-up in Patients With Heart Failure.","HERO","Inclusion Criteria:\n\n1. Patients aged ≥18 years old;\n2. Patients implanted with a cardiac defibrillator for less than 6 months, with or without resynchronization, enabling the HeartLogic™ algorithm;\n3. Patients with a history of HF (left ventricular ejection fraction ≤40%; or at least one episode of clinical HF with NT-proBNP blood concentration ≥450 ng\u002FL);\n4. Patients with New York Heart Association Class II or III HF;\n5. Patient able to comply with the protocol, including Latitude™ transmissions (including adequate connectivity), and study visits.\n6. Patients with compulsory health insurance\n\nExclusion Criteria:\n\n1. Patients not consenting and non-compliant with remote care directions.\n2. Patients with invasive remote HF monitoring device (such as CardioMems);\n3. Patients with a concomitant HF device other than cardiac resynchronization, such as a ventricular assist devices or cardiac contractility modulation devices;\n4. Patients on heart transplant list, or patients with a heart transplant;\n5. Patients with a glomerular filtration rate \\\u003C30 ml\u002Fmin\u002Fm2;\n6. Participation to a concomitant study evaluating management of HF decompensation, or diuretic titration.\n7. Patients enable to consent.\n8. Patients receiving State Medical Aid (Aide Médicale d'Etat).\n9. Pregnant or breastfeeding women.\n10. Persons benefiting from a reinforced protection, namely minors, persons deprived of liberty by a judicial or administrative decision, adults under legal protection, and finally patients in emergency situations","ALL","18 Years",{"count":219,"type":220},578,"ESTIMATED","INTERVENTIONAL",[223],"NA","This randomized, multicenter clinical trial will evaluate whether remote management guided by the HeartLogic™ algorithm improves outcomes compared with traditional face-to-face follow-up in adult patients with heart failure recently implanted with a HeartLogic™-enabled ICD or CRT-D device. The primary objective is to determine whether this strategy reduces, at 12 months, the proportion of patients with death, unscheduled hospitalization for heart failure, or deterioration in quality of life. Secondary objectives include assessment of hospitalization, mortality, quality of life, safety, and cost-effectiveness.",[226],"Heart Failure",[228,229,230,231,232],"heart failure","implantable cardioverter defibrillator","remote monitoring","hospitalization","quality of life","2026-06-19",{"date":235,"type":236},"2026-06-24","ACTUAL",{"date":238,"type":236},"2026-04-29",{"date":240,"type":220},"2029-05-15",{"name":5,"class":6},15]