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Airway Management clinical trials

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NCT ID: NCT04844723 Completed - Anesthesia Clinical Trials

Pediatric Videolaryngoscopic Intubation and Difficult Airway Classification

PeDiAC
Start date: April 12, 2021
Phase:
Study type: Observational

The study's primary aim is to develop and validate a multivariable diagnostic model for the prediction of difficult videolaryngoscopy (the 'PeDiAC classification') in children undergoing general anesthesia with tracheal intubation. The secondary aim is to compare the diagnostic performance of the PeDiAC-classification with the Cormack-Lehane classification.

NCT ID: NCT04769154 Completed - Intensive Care Unit Clinical Trials

Adult Airway Management in the Intensive Care Units and Regular Floors

Start date: March 2, 2021
Phase:
Study type: Observational [Patient Registry]

The goal of this descriptive observational study is to assess the success rate of endotracheal intubation at first attempt outside the operating room with direct laryngoscopy or with the use of an assisting device and identify adverse events; mainly hypoxemia (SpO2 < 85%), hypotension (SBP < 80 mmHg), and cardiac arrest in patients requiring elective or emergent endotracheal intubation. The main question it aims to answer is whether endotracheal intubation outside the OR at AUBMC has higher success rates and lower complication rates as compared to the literature. Participants will be evaluated according to the inclusion criteria and data extraction will be performed from the electronic health record (EHR). Researchers will compare success and complication rates with previous literature and international benchmarks.

NCT ID: NCT04724408 Completed - Airway Management Clinical Trials

VieScope Versus Direct Laryngoscopic Intubation

VieScOP
Start date: January 26, 2021
Phase: N/A
Study type: Interventional

Patients requiring endotracheal intubation for elective surgery without expected difficult airway are randomized to be intubated either by a) VieScope or b) conventional direct laryngoscopy.

NCT ID: NCT04680169 Completed - Airway Management Clinical Trials

I-gel vs AuraGain for Bronchoscopic Intubation Through SGA

Start date: January 18, 2021
Phase: N/A
Study type: Interventional

This trial compares two different second generation supraglottic airway devices (AuraGain and I-gel) used as a conduit for bronchoscopic tracheal intubation during continuous oxygenation in order tο determine time to successful tracheal intubation and ease of use.

NCT ID: NCT04582227 Completed - Airway Management Clinical Trials

Using Ambu Aura-i Laryngeal Mask Airway in Cranial Surgery

Start date: December 1, 2020
Phase:
Study type: Observational [Patient Registry]

the investigators hypothesize that Ambu aura-i LMA can be used safely in patients undergoing craniotomies and are effective in reducing the incidence of emergence hypertension.

NCT ID: NCT04564105 Completed - Airway Management Clinical Trials

Simulation Training and Teamwork Concerning Intubation on the Icu

Start date: September 4, 2020
Phase: N/A
Study type: Interventional

To assess effects of the simulation education on the group intubating patients in the iCU, in this prospective study investigators will video-record real-life intubations and simulations. From videos will be assessed correlation of technical and non-technical skills before and after the education and performance in real-life vs simulation intubation.

NCT ID: NCT04501692 Completed - Airway Management Clinical Trials

VivaSight-SL Versus Videolaryngoscopy in Expected Difficult Airway

VivaOP
Start date: August 27, 2020
Phase: N/A
Study type: Interventional

Patients requiring endotracheal intubation for elective surgery with an expected difficult airway are randomized to be intubated either by a) videolaryngoscopy or b) an endotracheal tube-mounted camera.

NCT ID: NCT04449042 Completed - COVID19 Clinical Trials

The PAWS-COVID-19 (Pediatric AirWay complicationS COVID-19) Registry

Start date: April 1, 2020
Phase:
Study type: Observational [Patient Registry]

The COVID-19 pandemic has disrupted anesthesia care all over the world. There remains very little data on current practice patterns and patient outcomes, particularly in anesthetized children. This is a prospective observational, multi-center study to investigate airway management related outcomes in children undergoing anesthesia during this pandemic. The investigators will compare the incidence of complications (particularly hypoxemia) in patients with COVID-19 to those who are COVID-19 negative during airway management. PAWS COVID-19 Registry https://is.gd/PEDICOVID19 Registration link https://is.gd/researchrequest

NCT ID: NCT04410289 Completed - Children, Only Clinical Trials

Defining the 'Sniffing Position" in Infants and Toddlers - A Pilot Study

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The "sniffing position" is widely accepted as a favorable position for direct laryngoscopy (DL) in both pediatric and adult patients. External anatomical markers are well documented to confirm proper 'sniffing position' in adults, but data on their use in the pediatric population is sparse. The investigators propose to define these markers in young children and investigate whether patients positioned using this standardized approach have better intubating conditions than those positioned randomly per the preference of the anesthesiologist.

NCT ID: NCT04343014 Completed - Airway Management Clinical Trials

Tongue Root Retractor For Fibroscopic Intubation

TRFI
Start date: March 10, 2016
Phase: N/A
Study type: Interventional

Patients admit to the operation rooms of First Affiliated Hospital of Nanjing Medical University and requiring endotracheal intubation for general anesthesia will be enrolled in this case controlled study. Patients 1) aged 18 to 70 years; 2) ASA graded I~II class; 3) general anesthesia should be performed under endotracheal intubation, will be included from this study. Patients 1) with organ transplant operations; 2) with thoracic and cardiac vascular surgery; 3) with severe heart or lung disease; 4) BMI over 35kg/m2, will be excluded from this study. The primary aim is to compare airway clearance for fibreoptic tracheal intubation in each patient position. Secondary outcomes include times to view the vocal cord and carina, the time for tube advancement through the vocal cords, as well as the total time to achieve tracheal intubation.Two anesthesiologists with 5 years of experience in conventional endotracheal intubation and trained for fibreoptic intubation will perform the maneuvers.