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Tracheal Intubation clinical trials

View clinical trials related to Tracheal Intubation.

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NCT ID: NCT05909215 Completed - Clinical trials for Hemodynamic Instability

Attenuation Of Hemodynamic Response To Laryngoscopy. Role Of Dexmedetomidine. A Dose Finding Study

Start date: August 23, 2021
Phase: Phase 4
Study type: Interventional

Two doses of Dexmedetomidine (0.5 µ/kg and 0.75 µ/kg) will be used to attenuate the stress response to laryngoscopy in American Society of Anesthesiology, physical class I patients which will be compared with the placebo-controlled group.

NCT ID: NCT05160207 Completed - Airway Management Clinical Trials

Intubation-induced Decrease in Heart Rate as an Indicator for Intraoperative Bradycardia

Start date: November 4, 2021
Phase:
Study type: Observational

This prospective observational study aims to determine, if an tracheal intubation-related decrease in heart rate is associated with intraoperative reflex bradycardia in patients undergoing microlaryngoscopy (MLS) in general anesthesia.

NCT ID: NCT04363775 Completed - Infection Clinical Trials

Comparison of VieScope vs. Macintosh Laryngoscope for Intubation in Level Cpersonal Protective Equipment Conditions

Start date: January 20, 2020
Phase: N/A
Study type: Interventional

The current COVID-19 pandemic, this is especially since the transmission of SARS-CoV-2 is thought to occur mainly through respiratory droplets generated by coughing and sneezing, by direct contact with contaminated surfaces and because in a large number of patients COVID-19 disease may be asymptomatic. As recommended by the CDC for aerosol-generating procedures (AGP), medical personnel should be equipped with full personal protective equipment (PPE) for AGP. Therefore, it is reasonable to search for the most effective methods of intubation in those conditions.

NCT ID: NCT04346459 Completed - Tracheal Intubation Clinical Trials

Three Different Techniques for Tracheal Intubation Via Supraglottic Airway Devices

Start date: January 10, 2020
Phase: N/A
Study type: Interventional

This study compares three different supraglottic airway devices used as a conduit for tracheal intubation in order το determine which one achieves the highest success rate of first attempt intubation

NCT ID: NCT04091568 Completed - Clinical trials for Intubation;Difficult

Patient Experience Following Awake Fibreoptic Intubation Compared to Asleep Fibreoptic Intubation

Start date: October 10, 2019
Phase:
Study type: Observational

The aim of this observational study is to explore and compare patients' experiences of asleep and awake fibreoptic intubation using a semi qualitative patient questionnaire. In particular, investigators will investigate the occurrence of negative experiences, such as distress and discomfort.

NCT ID: NCT03930550 Completed - Tracheal Intubation Clinical Trials

Infrared Transillumination of the Front of the Neck

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

Infrared light is applied to the front of the neck of patients for awake flexible optical intubation. The infrared light can be detected by the camera at the tip of the flexible video-bronchoscope. The flexible scope is introduced into the trachea with or without the aid of the blinking infra red light and the ease of placement of the flexible scope is studied.

NCT ID: NCT03874403 Completed - Tracheal Intubation Clinical Trials

Anesthetic Component Research on VATS and NIVATS

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

The non-intubated video-assisted thoracic surgery (NIVATS) can avoid intubation-related complications and for a smoother postoperative recovery. Successful results are accumulating not only from anecdotal case reports of difficult and high-risk patients not suitable for an intubated general anesthesia. However, in spite of safety and feasibility, there were still three main concerns: 1. how to maintain spontaneous breathing with optimal anesthetic depth; 2. How to analyze the components of general anesthesia and regional anesthesia; 3.what's the benefits on the recovery and the risk of aspiration risk with NIVATS? The traditional monitor or methods such as BIS system, SpO2, and follow-up aspiration signs could not offer sufficient evidence to resolve the three main concerns. Recently, there have been many new methods to monitor these concerns. The density spectral array (DSA) BIS system could analyze the change of the anesthetic component. The ORI is a dimensionless index that reflects oxygenation in the moderate hyperoxic range (PaO2 100-200 mmHg).

NCT ID: NCT03693235 Completed - Tracheal Intubation Clinical Trials

Adequate Bending Angle of a Lightwand

Start date: November 14, 2018
Phase: N/A
Study type: Interventional

For tracheal intubation with a lightwand, adequate bending angle was not exactly investigated. The purpose of the study is compare three bending angles of lightwands for safe and efficient tracheal intubation.

NCT ID: NCT03045094 Completed - Tracheal Intubation Clinical Trials

Neck Movement Implicate the Tracheal Tube-tip Displacement in Pediatric Surgery

Start date: March 20, 2017
Phase:
Study type: Observational

This study evaluates the effect of head and neck movement in children on endotracheal tube (ETT) tip displacement undergoing head-and-neck surgeries. The tube-tip displacement will be measured using flexible fiberoptic bronchoscope.

NCT ID: NCT02590237 Completed - Tracheal Intubation Clinical Trials

KingVision Video Laryngoscopy vs Direct Laryngoscopy - Equivalence Trial

Start date: October 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the Ambu KingVision videolaryngoscope performs as well as direct laryngoscopy for intubating small children and infants.