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Intubation; Difficult or Failed clinical trials

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NCT ID: NCT06011967 Completed - Clinical trials for Intubation; Difficult or Failed

Intubation With Different Angles of the Intubation Tube Using C-macr d Blade Videolaringoscope;

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

In this study we compared the intubation success, time needed for intubation, subglottic damage, postoperaitve sore throat, hoarseness and hemodynamic response to orotracheal intubation using three different intubation stylets with C-MAC R videolaryngoscope D- blade.

NCT ID: NCT06002815 Recruiting - Clinical trials for Intubation; Difficult or Failed

Comparison of Nasogastric Tube Insertion Success in Difficult and Easy Airway Patients

Start date: August 28, 2023
Phase:
Study type: Observational [Patient Registry]

This research aims to investigate potential variations in the success rate and occurrence of complications during nasogastric tube insertion between Difficult and Easy Airway Patients.

NCT ID: NCT05968781 Recruiting - Clinical trials for Intubation; Difficult or Failed

Predictive Factors for Successful Videolaryngoscopic Intubation Without Stylet

Start date: August 22, 2023
Phase:
Study type: Observational

The investigators aimed to evaluate the predictive factors for successful videolaryngoscopic intubation without stylet.

NCT ID: NCT05954533 Recruiting - Clinical trials for Intubation Complication

HEAVEN CRITERIA vs Modified LEMON Score for Predicting Difficult Intubation

Start date: July 1, 2022
Phase:
Study type: Observational

Emergency tracheal intubation is a lifesaving procedure frequently performed on critically ill and injured patients in the emergency department (ED). Emergency intubations are more difficult than elective intubations in the operating room setting because of the sicker patient population with a limited physiologic reserve and less controlled setting in the ED. Indeed, the proportion of difficult intubation ranges from 10% to 27% in the ED setting , whereas the rate ranges from 1% to 9% of elective intubation in the anaesthesia setting. Because emerging evidence demonstrates that repeated intubation attempts are associated with an increased risk of adverse events, early recognition of difficulty intubation with a systematic use of rescue methods in ED patients is critical. The commonest airway prediction tool is the LEMON score. In the modified LEMON score "Mallampati" was excluded as it was not a pragmatic assessment in the ED. Existing difficult airway prediction tools were derived in the elective surgery environment and may not be applicable to emergency airway management. LEMON criteria was designed for preoperative clinical setting. Hence in this study we are observing if HEAVEN (H- Hypoxemia E - extremes of age A - anatomical abnormalities V - vomit/ blood / fluid E - Exsanguination/anaemia N - neck mobility issues) is a better tool for predicting difficult intubatio.

NCT ID: NCT05927519 Not yet recruiting - Obesity, Morbid Clinical Trials

Comparison of Airtraq in Class 2-3 Obese and Nonobese Men During Intubation: a Prospective Randomized Clinical Study

Start date: December 5, 2023
Phase: N/A
Study type: Interventional

Morbid obesity is a growing disease. Intubations of these patients mostly difficult. Video laryngoscopes have to be used during the intubation of these patients. The intubation of men is more complicated and difficult than obese women. There were no trials compared to the new video laryngoscopes in morbidly obese men. Patients will be divided into two groups; non-obese and klas 2-3 obese. Airtraq will be used for their intubation. The time for intubation will be the primary aim of this prospective randomized study. The insertion time, perioperative hemodynamic variables, and postoperative complications will also be recorded.

NCT ID: NCT05913492 Completed - Critical Illness Clinical Trials

Difficult Airway Simulation-based Training

Start date: July 1, 2022
Phase:
Study type: Observational

Difficult airways remain a significant problem in anaesthesia, intensive care and emergency medicine. Simulation-based training gives better outcomes compared to non-simulation and non-intervention education. However, it remains unclear how long the acquired skills are retained and how often simulation training should repeat. The study aimed to investigate the efficacy and skills retention in training for difficult airway management in anaesthesiologists. After ethical committee approval, we conducted a prospective control study at the postgraduate Department of Surgery, Anaesthesiology and Intensive Therapy (Bogomolets National Medical University) from July to December 2022. Anaesthesiologists who applied for the continuous medical education course "Difficult airways management" were involved in the study. The simulation room included a mannequin Laerdal SimMom Advanced Patient Simulator, vital monitor, anaesthesia station LEON and airway devices. Each volunteer went through two simulation scenarios of difficult airway management: 1) "cannot intubate, can ventilate" (CI), 2) "cannot intubate, cannot ventilate" (CICV) with the assistance of the training centre operator. The primary endpoints included: more than three laryngoscopy attempts; supraglottic airway attempt missing; call for help skip; failure to initiate a surgical airway (for the CICV scenario). Secondary endpoints included: time to call for help; mean duration of desaturation; use of bougie; use of video laryngoscope (Airtraq); mean number of intubation attempts; improper usage of equipment of equipment, time to initiation of surgical airway preparation; time to initiation of surgical airway ventilation.

NCT ID: NCT05884645 Active, not recruiting - Clinical trials for Intubation Complication

Video Intelligence intubaTION (VITION)

VITION
Start date: May 1, 2023
Phase:
Study type: Observational

This study aims to train an AI for video-directed endotracheal intubation (VITION) to recognise the anatomical structures of the upper airway during video-directed endotracheal intubations.

NCT ID: NCT05843565 Recruiting - Clinical trials for Intubation; Difficult or Failed

Standard Versus Hyperangulated Video Laryngoscopy Blades for Intubation in Neonates and Small Infants

Start date: June 14, 2023
Phase: N/A
Study type: Interventional

The goal of this prospective randomized cross over clinical trial is to compare the difference in the percentage of glottic opening (POGO) between two different video laryngoscopy blades, the hyperangulated Cobalt blade and the straight Miller blade in neonates or small infants with body weight ≤ 5 kg and age ≤ 3 months. The main questions it aims to answer are: - Is there a significant difference in the POGO using the standard Miller video laryngoscope blade versus the non-standard hyperangulated Cobalt video laryngoscope blade in neonates and small infants? - Are there significant differences in the first attempt success rate at intubation, the number of attempts, the time to successful intubation, the type of blade used for successful intubation, and the occurrence of adverse events during intubation, such as episodes of bradycardia or desaturation? 40 (20 in each group) neonates or small infants with body weight ≤ 5 kg or age ≤ 3 months will be enrolled in one of the two groups over 2 years of work. Researchers will compare the POGO and Cormack and Lehane (C&L) classification using the hyperangulated Cobalt blade versus the straight Miller blade to identify the technique that provides optimal glottic views and intubating conditions in this patient population, and thus improved patient's safety.

NCT ID: NCT05833347 Completed - Clinical trials for Intubation; Difficult or Failed

Evaluation of Difficult Laryngoscopy With Ultrasonography in Pediatric Patients

Start date: May 10, 2023
Phase:
Study type: Observational

Pediatric patients pose challenges in airway management due to anatomical and physiological changes. Using recommended predictive tests for predicting difficult airway can be improved by combining them with ultrasound measurement of the anterior soft tissues of the neck. In this study, the investigators aim to evaluate the ultrasound measurement of anterior neck soft tissues in paediatric patients before anesthesia induction, to anticipate difficult laryngoscopy.

NCT ID: NCT05762068 Completed - Critical Illness Clinical Trials

Expert Consensus Statements for the Management of a Physiologically Difficult Airway Using the Delphi Method (PDADelphi)

PDADelphi
Start date: April 1, 2023
Phase:
Study type: Observational

The aim of this study is to review/identify the existing definition and management strategies for a physiologically difficult airway (PDA), to generate expert consensus on the various aspects of managing a patient with a PDA using the Delphi method, and to provide guidance to clinicians worldwide on safe tracheal intubation practices in patients with PDA to help improve patient outcomes.