Clinical Trials Logo

Intubation Complication clinical trials

View clinical trials related to Intubation Complication.

Filter by:

NCT ID: NCT02729610 Not yet recruiting - Clinical trials for Intubation Complication

Bronchial Blocker for One-lung Ventilation in Cardiac Surgery

Start date: March 2016
Phase: Phase 4
Study type: Interventional

To investigate if bronchial blocker is more suitable for one-lung ventilation during thoracoscope assisted mitral valve replacement surgery with Cardiopulmonary Bypass than the double-lumen endobronchial tube.

NCT ID: NCT02598609 Completed - Clinical trials for Intubation Complication

SEPREVEN: a Stepped-wedge Randomised Controlled Trial

SEPREVEN
Start date: November 23, 2015
Phase: N/A
Study type: Interventional

Adverse events are frequent in Neonatal Intensive Care Units' (NICU) patients and account for a high morbidity and mortality. Possible severe adverse events are central line associated bloodstream infections (CLABSI), ventilator and catheter associated adverse events and medication errors. Severity of the patient's outcome after an adverse event can be classified using the National Coordinating Council for Medication Error Reporting and Preventing (NCC MERP) Index for categorizing medication errors. The study will test the hypothesis that rates of adverse events in NICU patients will be reduced by the implementation of an educational program for the NICU caregivers (nurses and physicians), consisting of strategies for recognizing and preventing adverse events in their unit. These strategies will be oriented to prevent CLABSI, medication errors, skin and nasal complications and ventilator and catheter-associated adverse events. This trial has a stepped wedge cluster design, in which the NICUs from 12 hospitals in France will be randomized to the timing of implementation of the educational program. In order to describe the adverse events occurring during the study period, an anonymous voluntary adverse event reporting system will be provided to the caregivers of the participating units. A nested study will examine how caregivers communicate with the patients' parents in case of adverse event (disclosure or not, and caregivers' reasons). The rates of adverse events will be measured retrospectively using a neonatal NICU trigger tool.

NCT ID: NCT02495259 Terminated - Clinical trials for Intubation Complication

Comparison of Double Lumen Tube Placement Techniques

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

The purpose of this study is to compare three different standard of care methods of double-lumen endobronchial tube (DLT) placement in patients who are scheduled to have thoracic surgery in which lung isolation is required.

NCT ID: NCT02493478 Recruiting - Clinical trials for Intubation Complication

Improving Safety and Quality of Tracheal Intubation Practice in Pediatric ICUs

NEAR4KIDs
Start date: March 2010
Phase:
Study type: Observational

Advanced airway interventions are common high risk, high stakes events for children in intensive care units (ICU) and emergency departments (ED), with risk for life and health threatening consequences.

NCT ID: NCT02484352 Completed - Blood Pressure Clinical Trials

Optimal Dose of Intravenous Oxycodone for Endotracheal Intubation

Start date: July 2015
Phase: Phase 4
Study type: Interventional

Intravenous form of oxycodone is recently used for the adjunct of anesthetic agents to avoid adverse effects of the stimulation of endotracheal intubation. The potency ratio of oxycodone to fentanyl is not absolutely defined. The aim of this study was to assess the optimal dose of intravenous oxycodone for attenuation of hemodynamic responses to laryngoscopy and endotracheal intubation. A prospective, randomized, double-blind study was conducted. Ninety one patients were randomly divided into 5 group based on the dose of oxycodone; 0, 0.05, 0.1, 0.15, 0.2 mg/kg. After giving each assigned dose of intravenous oxycodone, anesthesia was induced with thiopental and rocuronium. Heart rate (HR) and blood pressure (BP) was collected at baseline, before intubation, 1, 2, 3 minutes after intubation. The change of BP was calculated by (highest BP after intubation - baseline BP)/baseline BP.

NCT ID: NCT02474394 Completed - Clinical trials for Intubation Complication

Effects of Videolaryngoscope on Intraocular Pressure

Start date: February 2013
Phase: Phase 4
Study type: Interventional

This study is designed to compare the effects of the McGrath Series 5 video laryngoscope and Macintosh laryngoscope on intraocular pressure during laryngoscopy.

NCT ID: NCT02364622 Completed - Clinical trials for Intubation Complication

The Effects of Flexible Intubating Stylet in the Accurate Placement of Double-lumen Endobronchial Tube

Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether using the flexible Trachway(R) intubating stylet could facilitate and promote the accurate placement of double-lumen endobronchial tube.

NCT ID: NCT02359370 Completed - Clinical trials for Intubation Complication

The Effects of Lidocaine and Magnesium Sulphate on the Attenuation of the Hemodynamic Response to Tracheal Intubation

Start date: September 2014
Phase: Phase 4
Study type: Interventional

Justification and Objectives: The hemodynamic response to stimuli of the airways is a common phenomenon and its control is important to decrease systemic repercussions. The objective of this study is to compare the effects of intravenous administration of Magnesium Sulphate versus Lidocaine in the hemodynamics of this reflex after laryngoscopy and tracheal intubation. Methods: This double blind, randomized, single center, and prospective study evaluated 56 patients, ASA 1 or 2, aged between 18 and 65 years, scheduled for elective surgeries under general anesthesia with tracheal intubation. Patients were divided into two groups. Group M received 30mg/kg of Magnesium Sulphate, and group L 2 mg/kg of Lidocaine through continuous infusion, immediately before induction of anesthesia. The values for blood pressure (BP), heart rate (HR) and bispectral index (BIS) were measured in both groups at six distinct moments related to the administration of the drugs under study.

NCT ID: NCT02329041 Completed - Clinical trials for Intubation Complication

Comparison of McGrath Series 5 and Airtraq Videolaryngoscope for Double-lumen Tube (DLT) Intubation

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

Previous study showed that McGrath Series 5 videolaryngoscope is an alternative tool for double-lumen tube intubation. We have compared it with traditional Macintosh laryngoscopefor double-lumen tube intubation. In this study, we will investigate its role in double-lumen tube intubation by comparison with another videolarygoscope.

NCT ID: NCT02326896 Completed - Clinical trials for Intubation; Difficult

MACOCHA Score Predicts Intubation Failure

Start date: November 2013
Phase: N/A
Study type: Observational

Risk factors for difficult intubation are well described in anesthesiology. But intubation in the intensive care unit (ICU) is a challenging issue, associated with severe life-threatening complications. Non-anesthesiologist trainees performing ICU intubation may not fully appreciate the potential difficulty and complications. Therefore in this retrospective analysis the MACOCHA score will be used to determine difficult intubation in the ICU and predict intubation failure.