[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"endotracheal-intubation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:endotracheal-intubation":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,53,77,110,131,154,190,222,245,270,294],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100650350","novel-integrated-tube-bougie-prototype-for-endotracheal-intubation-in-airway-simulation-100650350",false,"NCT07747922","Novel Integrated Tube-Bougie Prototype for Endotracheal Intubation in Airway Simulation","A Prospective Randomized Crossover Simulation Study Comparing an Integrated Tube-Bougie Prototype With Standard Stilet-Assisted and Gum Elastic Bougie Assisted Endotracheal Intubation","ITBP","Inclusion Criteria:\n\n* Professional Status: Being an Emergency Medicine Resident actively undergoing specialty training at the University of Health Sciences, Kocaeli City Hospital, Department of Emergency Medicine.\n* Voluntary Participation: Voluntarily agreeing to participate in the study and providing written informed consent prior to enrollment.\n* Postgraduate year (PGY) 1-4 residents.\n* Willing and able to provide written informed consent.\n\nExclusion Criteria:\n\n* Refusal to Participate: Declining to participate or refusing to provide written informed consent.\n* Physical or Neurological Limitations: Having any pre-existing physical, motor, or neurological impairment that could interfere with manual dexterity, procedural performance, or airway management simulation (e.g., hand injuries, tremors, etc.).\n* Inability to complete all study procedures.",true,"ALL","18 Years",{"count":21,"type":22},40,"ESTIMATED","INTERVENTIONAL",[25],"NA","Endotracheal intubation is a critical airway management procedure that frequently requires adjunctive devices, such as stylets or elastic bougies, to facilitate successful tube placement. Although videolaryngoscopy has become increasingly common, access to videolaryngoscopes remains limited in certain clinical settings, particularly in prehospital and resource-constrained environments. Consequently, stylets and bougies continue to play an essential role in airway management. To address this need, we developed a novel integrated tube-bougie prototype that combines the guidance function of an elastic bougie with an endotracheal tube into a single device.\n\nThis prospective, randomized, crossover simulation study is designed to compare the performance of the integrated tube-bougie prototype with conventional stylet-assisted and elastic bougie-assisted endotracheal intubation. Emergency medicine residents will perform intubations using all three techniques in both normal and difficult airway simulation scenarios according to a randomized crossover sequence.\n\nThe primary outcome is the time to successful endotracheal intubation. Secondary outcomes include first-attempt intubation success, perceived procedural difficulty assessed using a visual analog scale (VAS), incidence of esophageal intubation, dental trauma, and evaluation of the learning curve using cumulative sum (CUSUM) analysis.\n\nThe findings could contribute to the development of alternative airway assistive equipment for emergency airway management and training.",[28,29,30],"Airway Management","Endotracheal Intubation","Difficult Airway",[30,29,28,32,33,34,35,36,37,38,39],"Emergency Medicine","Simulation","Manikin","Bougie","Gum Elastic Bougie","Stylet","EPATS","Medical Education","NOT_YET_RECRUITING","2026-07-31",{"date":43,"type":44},"2026-08-05","ACTUAL",{"date":46,"type":22},"2026-08-10",{"date":48,"type":22},"2026-08-30",{"name":50,"class":51},"Huseyin Cahit Halhalli, MD","OTHER_GOV",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100648512","comparison-of-high-flow-nasal-cannula-and-tight-face-mask-for-maintaining-oxygenation-during-rapid-sequence-induction-100648512","NCT07723430","Comparison of High-Flow Nasal Cannula and Tight Face Mask for Maintaining Oxygenation During Rapid Sequence Induction","Comparison of the Effectiveness of High-Flow Oxygen Cannula Versus Tight Face Mask in Maintaining Oxygenation During Rapid Sequence Induction","Inclusion Criteria:\n\n* Adults aged 18 years or older.\n* Patients requiring rapid sequence induction (RSI) for endotracheal intubation in the operating room, emergency department, or intensive care unit.\n* Patients in whom both high-flow nasal cannula (HFNC) and tight face mask preoxygenation are technically feasible.\n* Patients (or their legally authorized representatives, when applicable) able to provide written informed consent.\n\nExclusion Criteria:\n\n* Patients requiring immediate crash intubation without sufficient time for preoxygenation.\n* Patients with facial deformities, upper airway obstruction, or other conditions preventing the use of either HFNC or a tight face mask.\n* Known contraindications or hypersensitivity to medications used for rapid sequence induction.\n* Pregnant women.\n* Patients younger than 18 years of age.\n* Patients with do-not-intubate (DNI) orders.\n* Patients already intubated or mechanically ventilated before enrollment.\n* Patients who underwent endotracheal intubation within the previous 24 hours.",{"count":61,"type":22},290,[25],"This prospective randomized controlled trial aims to compare the effectiveness of High-Flow Nasal Cannula (HFNC) versus Tight Face Mask (TFM) in maintaining oxygenation during rapid sequence induction (RSI) for endotracheal intubation in adult patients. Participants will be randomly assigned in a 1:1 ratio to receive either HFNC or TFM for preoxygenation before induction of anesthesia. The primary outcome is the lowest peripheral oxygen saturation (SpO₂) recorded from induction until successful endotracheal intubation. Secondary outcomes include the incidence of oxygen desaturation (\\\u003C90%), duration of apnea, duration of laryngoscopy, intubation time, number of intubation attempts, and peri-intubation complications. The study will determine whether HFNC provides superior oxygenation compared with conventional face mask preoxygenation during RSI and may contribute to improving airway management protocols and patient safety.",[65,28,29,66],"Hypoxemia","Rapid Sequence Induction","2026-07-22",{"date":69,"type":44},"2026-07-23",{"date":71,"type":22},"2026-08-01",{"date":73,"type":22},"2027-02-20",{"name":75,"class":76},"Khyber Teaching Hospital","OTHER",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":23,"phases":87,"briefSummary":88,"conditions":89,"keywords":92,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":107,"leadSponsor":108,"locationsCount":52},"100647255","bronchoscopic-versus-airway-exchange-catheter-guided-endotracheal-tube-exchange-100647255","NCT07706309","Bronchoscopic Versus Airway Exchange Catheter-Guided Endotracheal Tube Exchange","Bronchoscopic Endotracheal Tube Exchange as an Alternative to Airway Exchange Catheter-Guided Tube Exchange: A Prospective Study","Bronchex","Inclusion Criteria:\n\n* Human body donor preserved using the Thiel embalming method.\n* Intact trachea without relevant postmortem or preparation-related lesions.\n* Documented consent for scientific use of the body and confirmation of anatomical suitability by the Institute of Anatomy.\n* Sufficient mobility of the neck, jaw, and laryngeal region to permit realistic tube-exchange maneuvers.\n\nExclusion Criteria:\n\n* Tumor or stenosis involving the larynx, trachea, or central airways.\n* Previous surgery or radiotherapy involving the larynx or oral cavity.\n* Previous pneumonectomy.\n* Previous tracheotomy or laryngectomy.\n* Inability to achieve safe or standardized positioning of the cadaver.\n* Incomplete consent documentation or unclear provenance.\n* Preservation using a fixation method other than the Thiel method.",{"count":86,"type":22},2,[25],"This prospective experimental study compares two methods for replacing an endotracheal tube in Thiel-embalmed body donors. The conventional method uses an airway exchange catheter based on the Seldinger technique, whereas the investigational method uses a flexible bronchoscope to provide direct visual guidance throughout the exchange.\n\nThe primary outcome is the duration of interrupted ventilation, measured from cessation of ventilation until ventilation is resumed through a correctly positioned replacement tube. Secondary outcomes include unsuccessful tube exchange requiring complete reintubation, duration of individual procedural steps, procedures lasting more than 60 seconds, use of additional rescue equipment, and unforeseen technical difficulties.\n\nBoth techniques will be performed in two Thiel-embalmed donated human bodies using an alternating sequence. Four experienced physicians will perform 40 tube exchanges per technique, resulting in a total of 80 procedures.",[90,28,29,91],"Endotracheal Tube Exchange","Reintubation",[93,94,95,96,97,98,99,100,101],"Airway exchange catheter","bronchoscopy","interventional pneumology","tube exchange","reintubation","endotracheal tube exchange","apnea time","airway management","critical care","RECRUITING","2026-07-10",{"date":105,"type":44},"2026-07-15",{"date":103,"type":44},{"date":103,"type":22},{"name":109,"class":76},"Léo Franchetti",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":23,"phases":119,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":52},"100640916","impact-of-via-ct-based-3d-printing-technology-on-success-rate-in-endotracheal-intubation-in-students-100640916","NCT07612995","Impact of Via CT-based 3D Printing Technology on Success Rate in Endotracheal Intubation in Students","Impact of Via CT-based 3D Models and 3D Printing Technology on Success Rate in Endotracheal Intubation in Undergraduate Medical Students-A Prospective Single-Center Study","Inclusion Criteria:\n\n* The only patients who were selected for the intubation were grade I and II according to the American Society of Anesthesiologists (ASA), non-obese and with good visualization of soft palate and uvula (Mallampati classification)\n\nExclusion Criteria:\n\n* no",{"count":118,"type":22},80,[25],"The objective of this project is to develop a tracheal intubation teaching curriculum covering both normal and difficult airways using CT three-dimensional imaging and 3D printing technologies, enabling trainees to intuitively learn anatomical knowledge, operational skills, and special handling techniques, and to evaluate the learning outcomes. The research content includes the establishment of airway models and the training of students. Trainees in Group A will be trained using the tracheal intubation curriculum independently developed in this project, while trainees in Group B will be trained using traditional teaching methods, where instructors explain the course content via PowerPoint, elaborate on key and difficult points, answer student questions, and provide a summary. The teaching content for both groups is identical. After the teaching session, the teaching effectiveness will be evaluated using the second part of the teaching assessment methods.",[29],"2026-05-21",{"date":124,"type":44},"2026-05-29",{"date":126,"type":22},"2026-05",{"date":128,"type":22},"2026-08",{"name":130,"class":76},"xiaojing wang",{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":136,"acronym":4,"eligibilityCriteria":137,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":138,"enrollmentInfo":139,"targetDuration":4,"studyType":23,"phases":141,"briefSummary":142,"conditions":143,"keywords":4,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":145,"lastUpdatePostDateStruct":146,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":152,"locationsCount":86},"100636673","provu-video-stylet-with-versus-without-the-fekry-airway-100636673","NCT07568743","ProVu Video Stylet With Versus Without the Fekry Airway","Comparison of Intubation Time and Performance Between the ProVu Video Stylet With Versus Without the Fekry Airway in Adults With Normal Airway: A Single-Blinded Randomized Controlled Trial","Inclusion Criteria:\n\n* • American Society of Anesthesiologists (ASA) physical status I, II.\n\n  * Patients scheduled for elective surgery requiring general anesthesia and orotracheal intubation of less than 2 hours duration .\n  * Ganzouri Airway score \\\u003C3.\n\nExclusion Criteria:\n\n* Patient with Active cardiac condition.\n\n  * Patient with airway congenital anomaly.\n  * Mallampati score III or IV.\n  * Body mass index (BMI) \\> 35 kg\u002Fm² (obesity).\n  * Limited cervical spine mobility.\n  * History of difficult intubation, upper airway surgery, or trauma.\n  * Facial or oropharyngeal deformities.\n  * Allergy or contraindication to study medications.\n  * Refusal to participate.","65 Years",{"count":140,"type":22},130,[25],"This study aimed to compare assisted intubation using the ProVu video stylet device passing through Fekry airway versus intubation without the use of Fekry airway .\n\nThe investigators hypothesized that endotracheal intubation assisted by ProVu video stylet using the Fekry airway as a conduit for intubation would improve the glottic visualization and the higher first attempt success rate when compared to endotracheal intubation assisted by ProVu video stylet without using the Fekry airway.",[29,144],"Video Rigid Stylet","2026-05-05",{"date":147,"type":44},"2026-05-08",{"date":149,"type":22},"2026-05-10",{"date":151,"type":22},"2026-10-10",{"name":153,"class":76},"Cairo University",{"id":155,"slug":156,"hasResults":11,"nctId":157,"briefTitle":158,"officialTitle":159,"acronym":160,"eligibilityCriteria":161,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":162,"targetDuration":4,"studyType":23,"phases":164,"briefSummary":165,"conditions":166,"keywords":171,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":180,"lastUpdatePostDateStruct":181,"startDateStruct":183,"completionDateStruct":185,"leadSponsor":187,"locationsCount":189},"100539984","mechanical-insufflation-exsufflation-and-hypertonic-saline-in-nosocomial-bacterial-respiratory-tract-infection-100539984","NCT06310941","Mechanical Insufflation-exsufflation and Hypertonic Saline in Nosocomial Bacterial Respiratory Tract Infection","Aspiration of Bronchial Secretions With Mechanical Insufflation-Exsufflation and Hypertonic Saline in Bacterial Nosocomial Tracheobronchitis and Pneumonia in Intubated Patients.","ABSENTA","Inclusion Criteria:\n\n* Signed informed consent\n* Nosocomial pneumonia (vHAP or VAP) or nosocomial tracheobronchitis\n* Intubated with a cuffed endotracheal tube or tracheostomy cannula.\n\nExclusion Criteria:\n\n* Ominous prognosis\n* Frank hemoptisis\n* Barotrauma (pneumothorax or pneumomediastinum)\n* Bronchospasm (patients on bronchodilators for previous bronchospasm may be included\n* Unstable thoracic cage\n* Suspected unmonitored intracraneal hypertension",{"count":163,"type":22},100,[25],"Multicenter, randomized open label clinical trial to evaluate IEM and HS as concomitant therapy for respiratory tract infection in patients under artificial ventilation in the ICU.\n\nLung infection is a serious complication that may occur during hospital stay and may need artificial respiration or even develop during artificial ventilation for other causes.\n\nCurrent specific treatment consists of intravenous antibiotics. The current study evaluated whether aspiration and drainage of infected sputum helps curing this severe complication and whether nebulized HS has additional benefits, like loosening of secretions, eradicating bacteria or reducing inflammation.",[167,168,169,170,29],"Nosocomial Infection","Nosocomial Pneumonia","Tracheobronchitis","Mechanical Ventilation Complication",[172,173,174,175,176,177,178,179],"mechanical insufflation-exsufflation","cough assist device","hypertonic saline","nosocomial respiratory tract infection","hospital-acquired pneumonia","tracheobronchitis","ventilator-associated pneumonia","nebulization","2025-03-21",{"date":182,"type":44},"2025-03-26",{"date":184,"type":22},"2026-01-01",{"date":186,"type":22},"2027-12-30",{"name":188,"class":76},"Hospital San Carlos, Madrid",8,{"id":191,"slug":192,"hasResults":11,"nctId":193,"briefTitle":194,"officialTitle":195,"acronym":196,"eligibilityCriteria":197,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":198,"enrollmentInfo":199,"targetDuration":4,"studyType":23,"phases":201,"briefSummary":202,"conditions":203,"keywords":209,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":213,"lastUpdatePostDateStruct":214,"startDateStruct":216,"completionDateStruct":218,"leadSponsor":220,"locationsCount":52},"100585164","an-educational-intervention-to-improve-the-success-of-intubation-in-newborns-using-a-video-laryngoscope-by-reducing-the-time-the-procedure-takes-100585164","NCT06898801","An Educational Intervention to Improve the Success of Intubation in Newborns Using a Video Laryngoscope by Reducing the Time the Procedure Takes.","Neonatal INtubation After \"Just-in-time\" Audiovisual Training: a Randomised Controlled Trial","NINJA","Inclusion Criteria:\n\nNeonates of any age or gestation who require endotracheal intubation in the Neonatal Intensive Care Unit in the National Maternity Hospital during the study period.\n\nExclusion Criteria:\n\n* Neonates with an upper airway malformation.\n* If it is deemed by the treating clinical team that the clinical scenario does not allow time for the intervention e.g. cardiac arrest","1 Year",{"count":200,"type":22},140,[25],"This research focuses on one of the most common problems in newborn medicine: breathing difficulties. Breathing problems are the most common reason for admission to our neonatal unit at the National Maternity Hospital. When a baby has serious breathing difficulty, inserting a breathing tube to place them on a ventilator can be lifesaving. A breathing tube must be placed through the vocal cords into the windpipe (trachea). A device called a laryngoscope is placed in a patients mouth to allow the doctor to see the vocal cords and insert the tube correctly.\n\nThe skill of placing this breathing tube (intubation) is important for doctors and specialists to learn so that they can confidently perform it in an emergency.\n\nIn the past, doctors had more opportunities during their training to learn and practice this with supervision from seniors. In recent years, babies, thankfully, need to be intubated less frequently and doctors working hours are better regulated. As a result, junior doctors have less chances to perform this skill. There is a need to improve how we teach the procedure of intubating babies to doctors in training to meet the needs of trainees today.\n\nThe investigators want to perform a study to help teach doctors in training how to perform intubation of a newborn using a video laryngoscope. The team are looking to assess if showing a short educational video to the doctor and team just before performing an intubation using a video laryngoscope will reduce the time the procedure takes. This is called a \"Just-in-Time\" video. The investigators aim to demonstrate a benefit by performing a randomised control trial. This means that when a baby requires intubation as decided by their treating doctors, the team will be randomly allocated to view a \"Just-in-Time\" video before performing the intubation or not. The investigators will then compare the two groups to see if there is a difference in the total time the procedure takes.",[204,29,205,206,207,208],"Respiratory Distress Syndrome, Newborn","Neonatal Intubation Performance","Prematurity","Neonate","Education, Medical",[210,211,212],"Just-in-Time","Neonatal intubation","Teaching","2025-03-20",{"date":215,"type":44},"2025-03-27",{"date":217,"type":22},"2025-03",{"date":219,"type":22},"2027-05",{"name":221,"class":76},"University College Dublin",{"id":223,"slug":224,"hasResults":11,"nctId":225,"briefTitle":226,"officialTitle":227,"acronym":4,"eligibilityCriteria":228,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":229,"enrollmentInfo":230,"targetDuration":4,"studyType":23,"phases":231,"briefSummary":232,"conditions":233,"keywords":4,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":237,"lastUpdatePostDateStruct":238,"startDateStruct":239,"completionDateStruct":241,"leadSponsor":243,"locationsCount":52},"100535646","lidocaine-dexmedetomidine-esmolol-and-magnesium-effect-on-optic-nerve-sheath-diameter-after-laryngoscopy-100535646","NCT06254534","Lidocaine, Dexmedetomidine, Esmolol and Magnesium Effect on Optic Nerve Sheath Diameter After Laryngoscopy","Effect of Lidocaine, Dexmedetomidine, Esmolol and Magnesium Use on Optic Nerve Sheath Diameter and Hemodynamic Response After Laryngoscopy: Randomized, Controlled, Double-blind Trial","Inclusion Criteria:\n\n* Patients aged 18 to 80 years who will receive endotracheal intubation for general anesthesia and have an American Society of Anesthesiologists (ASA) Physical Status classification of I to III.\n\nExclusion Criteria:\n\n* Patients allergic to dexmedetomidine, esmolol, lidocaine, and magnesium; patients with uncontrolled hypertension or advanced heart failure with EF below 35%; patients with cardiac arrhythmia, especially Type 2 and 3 blocks, supraventricular arrhythmias. Patients with renal failure (GFR below 30) or severe liver failure; patients with known acute or previous intracranial pathology and known diagnosis of epilepsy, predefined difficult airway examination. Patients who required more than one attempt at intubation or total laryngoscopy took more than 20 seconds.","80 Years",{"count":163,"type":22},[25],"This clinical trial aims to compare the effects of lidocaine, dexmedetomidine, esmolol, and magnesium on optic nerve sheath diameter and hemodynamic response to laryngoscopy.\n\nThe participants will be patients determined to need intubation and general anesthesia for any elective surgery. Each participant will receive either lidocaine, dexmedetomidine, esmolol, magnesium, or none before anesthesia induction, according to randomization. The investigator will measure the optic nerve sheath diameter by ultrasonography before and after intubation. Researchers will compare the difference between optic nerve sheath diameter, systolic blood pressure, and heart rate before and after laryngoscopy and search for the most stable group. The trial aims to determine a general anesthesia induction protocol for patients sensitive to intracranial pressure changes reflected as optic nerve sheath diameter for easy monitoring.",[234,29,235,236],"Intracranial Hypertension","Optic Nerve Sheath Diameter","General Anesthesia","2025-03-16",{"date":213,"type":44},{"date":240,"type":44},"2024-02-14",{"date":242,"type":22},"2025-07",{"name":244,"class":76},"Haseki Training and Research Hospital",{"id":246,"slug":247,"hasResults":11,"nctId":248,"briefTitle":249,"officialTitle":250,"acronym":251,"eligibilityCriteria":252,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":253,"targetDuration":4,"studyType":255,"phases":4,"briefSummary":256,"conditions":257,"keywords":258,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":261,"lastUpdatePostDateStruct":262,"startDateStruct":264,"completionDateStruct":266,"leadSponsor":268,"locationsCount":52},"100559015","ed-airway-management-in-the-netherlands-100559015","NCT06558630","ED Airway Management in the Netherlands.","A Prospective Observational Cohort Study of Airway Management in Emergency Departments in the Netherlands.","DEAR","Inclusion Criteria:\n\n* All patients who undergo airway management in the ED.\n\nExclusion Criteria:\n\n* ED patients that undergo airway management outside of the ED (e.g. operation room), will be excluded",{"count":254,"type":22},1000,"OBSERVATIONAL","Airway management is one of the resuscitative procedures patients may undergo in the Emergency Department (ED). While this is a high risk procedure, to date there is no data available on airway management practices, success or safety in EDs in the Netherlands. The objective of this study is to describe airway management in the Netherlands.",[29],[259,260],"Emergency department","Airway management","2024-08-21",{"date":263,"type":44},"2024-08-23",{"date":265,"type":44},"2024-01-01",{"date":267,"type":22},"2027-01-01",{"name":269,"class":76},"Frisius Medisch Centrum",{"id":271,"slug":272,"hasResults":11,"nctId":273,"briefTitle":274,"officialTitle":275,"acronym":4,"eligibilityCriteria":276,"healthyVolunteers":17,"sex":18,"minAge":277,"maxAge":4,"enrollmentInfo":278,"targetDuration":4,"studyType":23,"phases":280,"briefSummary":281,"conditions":282,"keywords":283,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":285,"lastUpdatePostDateStruct":286,"startDateStruct":288,"completionDateStruct":290,"leadSponsor":292,"locationsCount":52},"100556481","stylet-shape-in-simulated-endotracheal-intubation-by-medical-students-100556481","NCT06525662","Stylet Shape in Simulated Endotracheal Intubation by Medical Students","Randomised Controlled Trial of Stylet Shape in Simulated Endotracheal Intubation by Medical Students","Inclusion Criteria:\n\n* Final year medical students in the Yong Loo Lin School of Medicine, National University of Singapore, undergoing their simulation posting. Endotracheal intubation is a procedure that is taught during this posting.\n\nExclusion Criteria:\n\n* Injuries precluding performance of endotracheal intubation. Non exhaustive examples include arm injuries.","21 Years",{"count":279,"type":22},268,[25],"Endotracheal intubation is a life saving procedure where a tube is placed into a person's windpipe to help them to breathe. This is a study of which shape of tube would lead to improved success in this procedure.",[29,39],[284,33],"Medical education","2024-07-24",{"date":287,"type":44},"2024-07-29",{"date":289,"type":44},"2024-07-10",{"date":291,"type":22},"2025-12-31",{"name":293,"class":76},"National University Hospital, Singapore",{"id":295,"slug":296,"hasResults":11,"nctId":297,"briefTitle":298,"officialTitle":299,"acronym":4,"eligibilityCriteria":300,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":301,"targetDuration":4,"studyType":255,"phases":4,"briefSummary":302,"conditions":303,"keywords":4,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":304,"lastUpdatePostDateStruct":305,"startDateStruct":307,"completionDateStruct":309,"leadSponsor":311,"locationsCount":52},"100544833","retrospective-study-of-airway-management-in-dutch-eds-100544833","NCT06374030","Retrospective Study of Airway Management in Dutch ED's","A Retrospective Study on the Practice and Safety of Airway Management in Dutch Emergency Departments","Inclusion Criteria:\n\n* All patients who underwent endotracheal intubation between 01-01-2019 and 31-12-2023 in the participating ED's\n\nExclusion Criteria:\n\n* Patients for which no information about the intubation can be found in the electronic patient chart will be excluded from the study.",{"count":254,"type":22},"Describing characteristics of the practice of airway management in Dutch emergency departments, including information about patient demographics, indications, performer characteristics, equipment and medication used and complications due to intubation.",[29],"2024-07-01",{"date":306,"type":44},"2024-07-03",{"date":308,"type":44},"2019-01-01",{"date":310,"type":22},"2024-12-31",{"name":269,"class":76}]