[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"awake-endotracheal-intubation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:awake-endotracheal-intubation":74},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":4,"eligibilityCriteria":13,"healthyVolunteers":10,"sex":14,"minAge":15,"maxAge":4,"enrollmentInfo":16,"targetDuration":4,"studyType":19,"phases":4,"briefSummary":20,"conditions":21,"keywords":23,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100637290",false,"NCT07574905","Evaluation of Satisfaction and Experiences in Patients Undergoing Awake Intubation.","Inclusion Criteria:\n\n* Be eligible for awake intubation\n* Agree to participate in the study\n* Be aged 18 or over\n\nExclusion Criteria:\n\n* Having communication difficulties.\n* Patients requiring emergency surgery.\n* Refusing to take part in the study.","ALL","18 Years",{"count":17,"type":18},100,"ESTIMATED","OBSERVATIONAL","The aim of this observational study is to evaluate postoperative satisfaction and experiences in patients undergoing awake intubation.",[22],"Awake Endotracheal Intubation",[24,25,26,27],"Awake intubation","Difficult airway","Satisfaction","Experience","RECRUITING","2026-05-05",{"date":31,"type":32},"2026-05-08","ACTUAL",{"date":34,"type":18},"2026-04-14",{"date":36,"type":18},"2026-06",{"name":38,"class":39},"Hacettepe University","OTHER",1,{"id":42,"slug":4,"hasResults":10,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":10,"sex":14,"minAge":15,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":59,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":69,"leadSponsor":71,"locationsCount":40},"100630220","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",{"count":49,"type":18},201,"INTERVENTIONAL",[52],"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.",[55,22,56,57,58],"Airway Management Assessment","Awake Fiberoptic Nasal Intubation","Videolaryngoscopy","Supraglottic Airway Device Insertion",[60,61,62,63],"videolaryngoscopy","awake tracheal intubation","fiberoptic bronchoscopy","aintree catheter","NOT_YET_RECRUITING","2026-03-18",{"date":67,"type":32},"2026-03-20",{"date":67,"type":18},{"date":70,"type":18},"2028-06-20",{"name":72,"class":73},"Kocaeli City Hospital","OTHER_GOV",""]