[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"atrial-fibrillation-rapid\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:atrial-fibrillation-rapid":33},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":5},"100325992","home-hospital-for-suddenly-ill-adults-100325992",false,"NCT03524222","Home Hospital for Suddenly Ill Adults","Home Hospital for Suddenly Ill Adults: A Clinical Trial","Inclusion Criteria:\n\n* Resides within either a 5-mile or 20 minute driving radius of emergency department\n* Has capacity to consent to study OR can assent to study and has proxy who can consent\n* \\>= 18 years-old\n* Can identify a potential caregiver who agrees to stay with patient for first 24 hours of admission. Caregiver must be competent to call care team if a problem is evident to her\u002Fhim. After 24 hours, this caregiver should be available for as-needed spot checks on the patient. This criterion may be waived for highly competent patients at the patient and clinician's discretion.\n* Primary or possible diagnosis of cellulitis, heart failure, complicated urinary tract infection, pneumonia, COPD\u002Fasthma, other infection, chronic kidney disease, malignant pain, diabetes and its complications, gout flare, hypertensive urgency, previously diagnosed atrial fibrillation with rapid ventricular response, anticoagulation needs, or a patient who desires only medical management that requires inpatient admission, as determined by the emergency room team.\n\nExclusion Criteria:\n\n* Undomiciled\n* No working heat (October-April), no working air conditioning if forecast \\> 80°F (June-September), or no running water\n* On methadone requiring daily pickup of medication\n* In police custody\n* Resides in facility that provides on-site medical care (e.g., skilled nursing facility)\n* Domestic violence screen positive\n* Acute delirium, as determined by the Confusion Assessment Method\n* Cannot establish peripheral access in emergency department (or access requires ultrasound guidance)\n* Secondary condition: end-stage renal disease, acute myocardial infarction, acute cerebral vascular accident, acute hemorrhage\n* Primary diagnosis requires multiple or routine administrations of intravenous narcotics for pain control\n* Cannot independently ambulate to bedside commode\n* As deemed by on-call medical doctor, patient likely to require any of the following procedures: computed tomography, magnetic resonance imaging, endoscopic procedure, blood transfusion, cardiac stress test, or surgery\n* High risk for clinical deterioration\n* Home hospital census is full (maximum 5 patients at any time)","ALL","18 Years",{"count":19,"type":20},3000,"ESTIMATED","INTERVENTIONAL",[23],"NA","The investigators propose a home hospital model of care that substitutes for treatment in an acute care hospital. Limited studies of the home hospital model have demonstrated that a sizeable proportion of acute care can be delivered in the home with equal quality and safety, reduced cost, and improved patient experience.",[26,27,28,29,30,31,32,33,34],"Infection","Heart Failure","COPD","Asthma","Gout Flare","Chronic Kidney Diseases","Hypertensive Urgency","Atrial Fibrillation Rapid","Anticoagulants; Increased","RECRUITING","2026-03-16",{"date":38,"type":39},"2026-03-17","ACTUAL",{"date":41,"type":39},"2018-01-18",{"date":43,"type":20},"2031-09",{"name":45,"class":46},"Brigham and Women's Hospital","OTHER",{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":68},"100520854","benefit-of-permanent-stimulation-of-the-left-branch-of-the-his-bundle-versus-right-ventricular-stimulation-after-atrioventricular-node-ablation-for-rapid-atrial-fibrillation-100520854","NCT06061978","Benefit of Permanent Stimulation of the Left Branch of the His Bundle Versus Right Ventricular Stimulation After Atrioventricular Node Ablation for Rapid Atrial Fibrillation","LEANA","Inclusion Criteria:\n\n1\u002F Pacemaker implanted patient with LBTP lead and back-up right ventricular lead who subsequently underwent successful atrioventricular node ablation for rapid AF 2) NAV ablation procedure performed less than 15 days ago 3) Age ≥ 18 years 4) Woman of childbearing age with effective contraception (estrogen-progestin or intrauterine device or tubal ligation) for at least 1 month and for the duration of the study, and a negative urine pregnancy test by B-HCG at inclusion Or, Postmenopausal woman: confirmatory diagnosis (non-medically induced amenorrhea for at least 12 months prior to the inclusion visit).\n\n5\\) Membership of a social security scheme 6) Patient follow-up feasible 7) Patient has read and understood the information leaflet and signed the informed consent form\n\nExclusion Criteria:\n\n1. Impairment of autonomy such that a maximal cardiorespiratory effort test (VO2 Max test) cannot be performed under good conditions (ADL scale \\\u003C 5).\n2. LVEF \\\u003C 40% at inclusion\n3. Person deprived of liberty by an administrative or judicial decision, or person under court protection, sub-guardianship or curatorship.\n4. Patient participating in another interventional trial\n5. Any history of illness or psychological or sensory abnormality likely to prevent the subject from fully understanding the conditions required for participation in the protocol, or from giving informed consent.\n6. Pregnant, parturient or breast-feeding women, or those without proven contraception",{"count":55,"type":20},60,[23],"The objective of the study is to evaluate the functional benefit of left bundle branch of His pacing compared to right ventricular pacing in patients implanted with a pacemaker prior to a atrioventricular node ablation procedure for rapid atrial fibrillation",[33],"2026-02-05",{"date":61,"type":39},"2026-02-10",{"date":63,"type":39},"2023-11-27",{"date":65,"type":20},"2027-05-27",{"name":67,"class":46},"University Hospital, Rouen",1]