Clinical trials: Supraglottic Airway Device Insertion
Appropriate Affect, Complication of Device Insertion
Requirements of Propofol With Target Controlled Infusions for Supraglottic Airway Devices
to evaluate and compare the effect-site concentration of propofol with the TCI system for second-generation SGA device insertion between the I-gel™, Supreme™, ProSeal™ and Laryngeal Tube Suction II™.
- Trial name
- NCT04664595
- Testing
- Propofol Fresenius
- Where
- 2 sites in Thailand
- Volunteers
- 40 people
- Sponsor
- Prince of Songkla University
General Anesthesia, Supraglottic Airway Device
The Accuracy of the Performance and Placement Test for Predicting Supraglottic Airway Device (SAD) Position in the Hypopharynx as Confirmed With Video Laryngoscopy
The supraglottic airway device (SAD) is currently widely used in patients undergoing general anaesthesia as a method of securing the airway.
- Conditions
- General Anesthesia, Supraglottic Airway Device, Laryngeal Mask Airway
- Trial name
- NCT03643029
- Testing
- Video-laryngoscopy following SAD insertion
- Volunteers
- 50 people
- Sponsor
- University of Malaya
Airway Obstruction
The Effect of Supraglottic Airway Insertion on the Accuracy of Cricothyroid Membrane Identification in Females
Prospective, observational, study that will examine if a sited supraglottic airway (the igel) will increase the accuracy of identifying the cricothyroid membrane in female patients.
- Trial name
- NCT03105037
- Where
- Ireland
- Volunteers
- 64 people
- Sponsor
- The Rotunda Hospital
Respiratory Distress Syndrome, Newborn
Feasibility Study of Placement and Surfactant Administration Through a Preterm Size Laryngeal Mask Airway in Very Low Birth Weight Neonates With Respiratory Distress Syndrome
Surfactant administration via a supraglottic airway device or laryngeal mask airway (SALSA) is a minimally invasive method of instilling surfactant in the trachea during spontaneous breathing and after applying nasal continuous…
- Trial name
- NCT06606444
- Testing
- Surfactant Administration Through Laryngeal or Supraglottic Airways
- Where
- Vietnam
- Volunteers
- 45 people
- Sponsor
- Karolinska Institutet
Airway Obstruction
Safety and Efficacy of the LMA Supreme When Inserted With Patients in the Prone Position
This study is a non-randomized, observational, non-comparative prospective study to evaluate the safety, efficacy and performance of the LMA Supreme laryngeal mask airway when used according to the device's Instructions for Use.
- Trial name
- LMA (NCT03633942)
- Testing
- LMA Supreme
- Where
- United States
- Volunteers
- 1,000 people, healthy volunteers welcome
- Sponsor
- Laser Spine Institute
Laryngeal Mask Airway, Children
Risk Factors for Pediatric Difficult Supraglottic Airway Placement and Ventilation
This study is designed to observe the occurrence of failure or difficulty during placement of supraglottic airway devices (SGAs) and its associated risk factors in pediatric patients.
- Conditions
- Laryngeal Mask Airway, Children, Airway Management
- Trial name
- PEDSGAP (NCT06073977)
- Where
- 6 sites in Turkey (Türkiye)
- Volunteers
- 3,750 people
- Sponsor
- Alper Kilicaslan
Airway Management
Artificial Intelligence-Assisted Ultrasound Assessment of Laryngeal Mask Airway Placement
This prospective observational study aims to develop and evaluate artificial intelligence-based models for the assessment of laryngeal mask airway (LMA) placement in adult patients undergoing elective surgery under general…
- Trial name
- NCT07766382
- Where
- Turkey (Türkiye)
- Volunteers
- 200 people
- Sponsor
- Duzce University
Laryngeal Mask Airways, Fiberoptic Bronchoscopy (FOB)
Fiberoptic Evaluation of i-Gel and Air-Q sp3G Supraglottic Airway Devices in Pediatric Patients
This single-center, prospective, randomized controlled study aims to compare the placement accuracy of iGel and Air-Q sp3G supraglottic airway (SGA) devices in pediatric patients aged 1-8 years undergoing elective surgery under…
- Conditions
- Laryngeal Mask Airways, Fiberoptic Bronchoscopy (FOB), Elective Surgeries, Gastric Insufflation
- Trial name
- NCT07141498
- Where
- Turkey (Türkiye)
- Volunteers
- 91 people, healthy volunteers welcome
- Sponsor
- Ankara City Hospital Bilkent