Endotracheal Intubation

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Review clinical trials related to Endotracheal Intubation. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Impact of Via CT-based 3D Printing Technology on Success Rate in Endotracheal Intubation in Students

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.

Participants needed: 80
Trial details
Biological sex: AllType: InterventionalSponsor: xiaojing wangUpdated: May 29, 2026Locations: 1
Eligibility criteria

The only patients who were selected for the intubation were grade I and II accor...

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Status: Recruiting

ProVu Video Stylet With Versus Without the Fekry Airway

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 . The 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.

Participants needed: 130
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: May 8, 2026Locations: 2
Eligibility criteria

• American Society of Anesthesiologists (ASA) physical status I, II. [+2]

Patient with Active cardiac condition. [+8]

Status: Not yet recruiting

Hyaluronic Acid for Prevention of Post-Intubation Sore Throat and Hoarseness

The goal of this clinical trial is to find out whether applying Endotra Gel, a hyaluronic acid-based gel, to the endotracheal tube can help reduce sore throat and hoarseness after surgery. These symptoms are common after general anesthesia when a endotracheal tube is placed into the trachea. They can cause discomfort and affect patient recovery. The main questions this study aims to answer are: * Does Endotra Gel reduce the chance of having a sore throat after surgery? * Does it help improve hoarseness or coughing after surgery? Participants in this study will: * Undergo general anesthesia for breast cancer surgery * Be randomly assigned to one of two groups: * One group will receive Endotra Gel applied to the endotracheal tube before intubation * The other group will have standard care with no gel * Be monitored for sore throat, hoarseness, and coughing right after surgery and on the day after surgery * Answer questions about their symptoms and satisfaction with their recovery The results will help researchers learn whether using Endotra Gel during intubation can improve patient comfort and reduce airway irritation after surgery.

Participants needed: 92
Trial details
Age: 19-80Biological sex: AllType: InterventionalSponsor: Pusan National University Yangsan HospitalUpdated: Jun 27, 2025
Eligibility criteria

Adults aged 19 to 80 years [+2]

Mallampati classification of III or higher [+5]

Status: Not yet recruiting

Mechanical Insufflation-exsufflation and Hypertonic Saline in Nosocomial Bacterial Respiratory Tract Infection

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. Lung 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. Current 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.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospital San Carlos, MadridUpdated: Mar 26, 2025Locations: 8
Eligibility criteria

Signed informed consent [+2]

Ominous prognosis [+5]

Status: Not yet recruiting

An Educational Intervention to Improve the Success of Intubation in Newborns Using a Video Laryngoscope by Reducing the Time the Procedure Takes.

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. The 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. In 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. The 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.

Participants needed: 140
Trial details
Age: Up to 1Biological sex: AllType: InterventionalSponsor: University College DublinUpdated: Mar 27, 2025Locations: 1
Eligibility criteria

Neonates with an upper airway malformation. [+1]

Status: Recruiting

Lidocaine, Dexmedetomidine, Esmolol and Magnesium Effect on Optic Nerve Sheath Diameter After Laryngoscopy

This clinical trial aims to compare the effects of lidocaine, dexmedetomidine, esmolol, and magnesium on optic nerve sheath diameter and hemodynamic response to laryngoscopy. The 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.

Participants needed: 100
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Haseki Training and Research HospitalUpdated: Mar 20, 2025Locations: 1
Eligibility criteria

Patients aged 18 to 80 years who will receive endotracheal intubation for genera...

Patients allergic to dexmedetomidine, esmolol, lidocaine, and magnesium; patient...

Status: Recruiting

ED Airway Management in the Netherlands.

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.

Participants needed: 1,000
Trial details
Biological sex: AllType: ObservationalSponsor: Frisius Medisch CentrumUpdated: Aug 23, 2024Locations: 1
Eligibility criteria

All patients who undergo airway management in the ED.

ED patients that undergo airway management outside of the ED (e.g. operation roo...

Status: Recruiting

Stylet Shape in Simulated Endotracheal Intubation by Medical Students

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.

Participants needed: 268
Trial details
Age: 21+Biological sex: AllType: InterventionalSponsor: National University Hospital, SingaporeUpdated: Jul 29, 2024Locations: 1
Eligibility criteria

Final year medical students in the Yong Loo Lin School of Medicine, National Uni...

Injuries precluding performance of endotracheal intubation. Non exhaustive examp...

Status: Recruiting

Retrospective Study of Airway Management in Dutch ED's

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.

Participants needed: 1,000
Trial details
Biological sex: AllType: ObservationalSponsor: Frisius Medisch CentrumUpdated: Jul 3, 2024Locations: 1
Eligibility criteria

All patients who underwent endotracheal intubation between 01-01-2019 and 31-12-...

Patients for which no information about the intubation can be found in the elect...