[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"device-usability\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:device-usability":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100607486","early-phase-1-clinical-evaluation-of-the-origin-intubation-system-100607486",false,"NCT07189182","Clinical Evaluation of the Origin Intubation System","Inclusion Criteria:\n\n1. Male or Female subjects 18 years of age or older and less than 75.\n2. English or Spanish Speaking.\n3. Undergoing elective surgery requiring endotracheal intubation.\n4. Use of general anesthesia.\n\nExclusion Criteria:\n\n1. Patients with high aspiration risk.\n2. Inability to provide informed consent in English or Spanish\n3. Patients for whom an awake intubation is indicated and planned.\n4. Patients with a history of head and neck radiation.\n5. Pregnant patients.\n6. Patients with BMI \\>35\n7. ASA 4 or higher\n8. Patients who the investigator deems ineligible at the investigator's discretion.\n9. Planned post-operative intubation.\n10. Current incarceration.",true,"ALL","18 Years","75 Years",{"count":20,"type":21},15,"ESTIMATED","INTERVENTIONAL",[24],"EARLY_PHASE1","There are currently two options that are utilized are artificial airways in the operating room as well in emergency medicine: the endotracheal tube and the supraglottic airway. However, with these devices, healthcare professionals often experience difficulty and\u002For failure in utilizing these devices during their first-pass at intubation. Additionally, military medics often forego intubation in favor of basic life support during prolonged resuscitation. This study aims to test a device, one that has been tested in over 100 cadavers, to determine if it is a viable and safer\u002Fmore successful option for intubation.",[27],"Device Usability",[29,30,31],"Intubation","General Anesthesia","Anesthesia","NOT_YET_RECRUITING","2026-04-22",{"date":35,"type":36},"2026-04-27","ACTUAL",{"date":38,"type":21},"2026-09-01",{"date":40,"type":21},"2027-09-01",{"name":42,"class":43},"Stanford University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":5},"100348072","a-feedback-enabled-magnetic-device-for-temporary-management-of-blepharoptosis-100348072","NCT03812016","A Feedback-enabled Magnetic Device for Temporary Management of Blepharoptosis","Comparison of Treatment Outcomes for Blepharoptosis of Various Etiologies Using a Feedback-enabled Magnetic Device","Inclusion Criteria:\n\n* Patients with ptosis; they are capable of understanding and complying with protocol requirements\n* Aged 18 years old or older\n\nExclusion Criteria:\n\n* Upper eyelid scar, contracture, or fibrosis due to previous surgical intervention(s)\n* Patients with psychiatric (or mental) disorders; they are unable to cooperate or follow the study procedure\n* Children younger than 18 years of age","85 Years",{"count":54,"type":21},40,[56],"NA","To develop a feedback-enabled magnetic device for management of blepharoptosis and evaluate its efficacy and safety, including the gain of palpebral fissure height, visual field obstruction, blurred vision, foreign body sensation over the cornea, burning or hot sensation over facial skin, and erythema or pruritus over the eyelid, by performing a human trial on patients with blepharoptosis.",[59,27],"Blepharoptosis",[59,61,62,63,64],"Blink restoration","Magnetic device","Oculomotor nerve palsy","Ptosis","RECRUITING","2025-05-11",{"date":68,"type":36},"2025-05-14",{"date":70,"type":36},"2023-04-01",{"date":72,"type":21},"2026-12-31",{"name":74,"class":43},"E-DA Hospital"]