[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"airway-management-assessment\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:airway-management-assessment":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100630220","comparison-of-awake-tracheal-intubation-methods-100630220",false,"NCT07484841","Comparison of Awake Tracheal Intubation Methods","A Comparison of Three Difficult Intubation Techniques in Patients With Anticipated Difficult Intubation: A Prospective, Randomized, Parallel-group Clinical Trial","ATI","Inclusion Criteria:\n\n* Adult patients aged 18 and older\n* Patients classified as ASA I-II according to the American Society of Anesthesiologists (ASA) classification\n* Patients scheduled for elective surgery\n* Patients expected to require difficult mask ventilation, difficult laryngoscopy, or difficult tracheal intubation; patients expected to have short apnea periods (Planjuan goiter); patients at risk of aspiration; patients expected to require difficult rescue techniques; and patients with a reported history of difficult intubation\n* Patients scheduled for intubation using the awake tracheal intubation (ATI) method\n* Individuals who have agreed to participate in the study by signing an informed consent form\n\nExclusion Criteria:\n\n* Patients with a mouth opening \\\u003C1.5 cm\n* Patients requiring emergency intubation or emergency surgery (situations where there is insufficient time to administer ATI)\n* Patients who cannot cooperate (mental incapacity, impaired consciousness, inability to communicate, etc.)\n* Patients with known allergies to lidocaine or other local\u002Ftopical anesthetic agents used\n* Pregnancy\n* Patients with a history of severe cardiac arrhythmia or hemodynamic instability (due to increased risk during intubation)\n* Patients who have previously undergone tracheostomy or whose airway is technically obstructed due to anatomical deformity\n* Patients who refuse to participate in the study or who do not provide informed consent","ALL","18 Years",{"count":20,"type":21},201,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aim of this study was to compare three different awake tracheal intubation technique\n\n-fiberoptic bronchoscopy (ATI:FB), videolaryngoscopy (ATI:VL), and fiberoptic bronchoscopy via a supraglottic airway device (ATI:SAD)- in terms of success rates, intubation times, and complications. Additionally, the study aims to evaluate the reliability of the SAD-assisted ATI method and its potential to contribute to the literature.",[27,28,29,30,31],"Airway Management Assessment","Awake Endotracheal Intubation","Awake Fiberoptic Nasal Intubation","Videolaryngoscopy","Supraglottic Airway Device Insertion",[33,34,35,36],"videolaryngoscopy","awake tracheal intubation","fiberoptic bronchoscopy","aintree catheter","NOT_YET_RECRUITING","2026-03-18",{"date":40,"type":41},"2026-03-20","ACTUAL",{"date":40,"type":21},{"date":44,"type":21},"2028-06-20",{"name":46,"class":47},"Kocaeli City Hospital","OTHER_GOV",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":48},"100595041","the-insertion-of-i-gel-and-classic-lma-in-different-head-positions-in-elderly-patients-100595041","NCT07027293","The Insertion of I-gel and Classic LMA in Different Head Positions in Elderly Patients","Evaluation of the Insertion of I-gel and Classic LMA in Different Head Positions in Elderly Patients","Inclusion Criteria:\n\n* ASA classification I-III\n* Age over 75 years\n\nExclusion Criteria:\n\n* Known or anticipated difficult airway\n* Contraindications for the use of a supraglottic airway device\n* Patients scheduled for endotracheal intubation","75 Years",{"count":58,"type":21},120,[24],"This prospective, randomized, double-blind clinical study aims to evaluate the insertion success of two supraglottic airway devices, the classic Laryngeal Mask Airway (LMA) and the I-gel, in different head and neck positions in elderly patients undergoing elective urological surgery under general anesthesia. A total of 120 patients aged over 75 years with ASA physical status I-III will be randomly assigned to one of four groups: standard position with I-gel, right lateral rotation with I-gel, standard position with classic LMA, and right lateral rotation with classic LMA. The study will compare insertion time, ease and success of placement, number of attempts, hemodynamic responses, oropharyngeal leak pressures, fiberoptic scores, and airway-related complications. The findings aim to provide clinical guidance on the optimal use of supraglottic airway devices in geriatric patients in various head positions.",[27,62,63,64],"Supraglottic Airways","Supraglottic Airways for General Anesthesia","Laryngeal Mask Airways",[66,67,68,69,70,71,72,73],"Supraglottic airway device","i-gel","Classic laryngeal mask airway","Elderly patients","Airway management","Head position","General anesthesia","Insertion success","RECRUITING","2025-09-10",{"date":77,"type":41},"2025-09-17",{"date":79,"type":41},"2025-06-20",{"date":81,"type":21},"2025-09-15",{"name":83,"class":84},"Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey","OTHER"]