[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100582677":3},{"organization":4,"armGroups":7,"interventions":17,"overallOfficials":10,"centralContacts":23,"locations":29,"responsibleParty":86,"collaborators":10,"id":88,"slug":89,"hasResults":90,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":94,"eligibilityCriteria":95,"healthyVolunteers":90,"sex":96,"minAge":10,"maxAge":10,"enrollmentInfo":97,"targetDuration":10,"studyType":100,"phases":10,"briefSummary":101,"conditions":102,"keywords":10,"overallStatus":32,"whyStopped":10,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":113},{"fullName":5,"class":6},"Phagenesis Ltd.","INDUSTRY",[8,12],{"label":9,"type":10,"description":11,"interventionNames":10},"Control Group",null,"Patient requires a nasogastric feeding tube for severe dysphagia and required dysphagia treatment",{"label":13,"type":10,"description":14,"interventionNames":15},"Treatment Group","Patients who have undergone PES treatment for severe dysphagia.",[16],"Device: 1. Phagenyx® System Group Patients",[18],{"type":19,"name":20,"description":21,"armGroupLabels":22,"otherNames":10},"DEVICE","1. Phagenyx® System Group Patients","Patients who have undergone Pharyngeal Electrical Stimulation (PES) treatment for severe dysphagia using the Phagenyx® System",[13],[24],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":28},"Jennifer Miller","CONTACT","248-420-3292","jennifer.miller@phagenesis.com",[30,52,69],{"facility":31,"status":32,"city":33,"state":34,"zip":35,"country":36,"countryCode":37,"cosmosGeoPoint":38,"geoPoint":43,"contacts":44},"Banner University Medical Center","RECRUITING","Phoenix","Arizona","85006","United States","US",{"type":39,"coordinates":40},"Point",[41,42],-112.07404,33.44838,{"lat":42,"lon":41},[45,49],{"name":46,"role":26,"phone":47,"phoneExt":10,"email":48},"Karla Granados","480-412-6859","granados13@arizona.edu",{"name":50,"role":51,"phone":10,"phoneExt":10,"email":10},"Andrei Alexandrov, MD","PRINCIPAL_INVESTIGATOR",{"facility":53,"status":32,"city":54,"state":55,"zip":56,"country":36,"countryCode":37,"cosmosGeoPoint":57,"geoPoint":61,"contacts":62},"HMH Jersey Shore University Medical Center","Neptune City","New Jersey","07753",{"type":39,"coordinates":58},[59,60],-74.02792,40.20011,{"lat":60,"lon":59},[63,67],{"name":64,"role":26,"phone":65,"phoneExt":10,"email":66},"Alexandria Nwar","732-776-3681","alexandria.nuwar@hmhn.org",{"name":68,"role":51,"phone":10,"phoneExt":10,"email":10},"Sanskriti Mishra, MD",{"facility":70,"status":32,"city":71,"state":72,"zip":73,"country":36,"countryCode":37,"cosmosGeoPoint":74,"geoPoint":78,"contacts":79},"University of Texas","Houston","Texas","77030",{"type":39,"coordinates":75},[76,77],-95.36327,29.76328,{"lat":77,"lon":76},[80,84],{"name":81,"role":26,"phone":82,"phoneExt":10,"email":83},"Elena Moreno","713-500-5638","Elena.Espino@uth.tmc.edu",{"name":85,"role":51,"phone":10,"phoneExt":10,"email":10},"Alex Choi, MD",{"type":87,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100582677","phagenyx-registry-study-100582677",false,"NCT06866418","Phagenyx® Registry Study","Phagenyx® Registry Study: Evaluating Swallowing Therapy Outcomes and Recovery in the U.S.","RESTORE-US","Inclusion Criteria:\n\n1. Phagenyx® System Group Patients: Patients underwent treatment with the Phagenyx® System for a minimum of 3 treatments.\n2. Control Group Patients: Patient requires a nasogastric feeding tube for severe dysphagia and required dysphagia treatment.\n3. Willing and able to provide appropriate informed consent (if required).\n\nExclusion Criteria:\n\n1. Primary endpoint outcome data not collected or not available.\n2. In the investigator or sponsor's opinion the patient is not considered suitable.\n3. Participation in another interventional study (medicinal or device) that could influence the outcomes of PES.\n4. Treatment of dysphagia with other forms of electrical stimulation.","ALL",{"count":98,"type":99},600,"ESTIMATED","OBSERVATIONAL","A retrospective, open-label, matched-control registry study designed to characterize the effectiveness of Pharyngeal Electrical Stimulation (PES) to improve swallowing in patients with severe dysphagia post stroke when delivered using the Phagenyx® System in real-world clinical settings in hospitals in the United States of America (US).",[103],"Dysphagia","2026-07-08",{"date":106,"type":107},"2026-07-09","ACTUAL",{"date":109,"type":107},"2025-09-15",{"date":111,"type":99},"2036-09",{"name":5,"class":6},3]