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Intubation Complication clinical trials

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NCT ID: NCT03846713 Recruiting - Clinical trials for Intubation Complication

Thermosoftening of Double-lumen Tube for Airway Exchanger Catheter

Start date: December 27, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of double-lumen tube thermal-softening before intubation on the success rate of tube exchange by airway exchange catheter.

NCT ID: NCT03808896 Recruiting - Clinical trials for Intubation Complication

TCHCCT-Zhong-Xing-Emergency-Department-airway-clincal (TTC)

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

In the previous study on mannekin, the investigators found stylet-assisted lifting of epiglottis is an useful technique on difficult airway (Cormack-Lehane grade IIIa, IIIb) without increasing subjective difficulty. It has no expenses other than the routine intubation process. Recently, the studies have proved that the bougie-assisted laryngoscopy can improve first pass intubation rate in the emergency department. However, bougie is a disposable device and may increased medical expenditure. The investigators will evaluate the safety of bougie and epiglottic lifting technique, as well as the first pass and overall success rate of intubation comparing to traditional video laryngoscopy and direct laryngoscopy.

NCT ID: NCT03770104 Recruiting - Clinical trials for Intubation Complication

Correct Endotracheal Tube Position in Newborns Intubated in the Delivery Room

Intubated-DR
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

The investigators wished to determine whether estimating endotracheal tube (ETT) insertion depth using the formula given by Spanish guidelines recommendations (5,5 plus weight) rather than the depth using the formula given by international guidelines recommendations (6 plus weight) resulted in more correctly positioned endotracheal tube tips in newborns intubated in the delivery room.

NCT ID: NCT03250975 Recruiting - Clinical trials for Intubation Complication

Incidence of Acute Laryngeal Injury Following Endotracheal Intubation

Start date: August 19, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this investigation is to delineate the incidence of acute and chronic laryngeal injury following intubation within our health system. In addition, this study seeks to identify risk factors for airway injury that may provide information to help reduce the incidence of injury or increase the speed of diagnosis through hospital based process measures. Study Aims 1. Determine the incidence of acute laryngeal injury in patients with prolonged intubation. 2. Determine the incidence of chronic laryngeal injury in the subset of patients with acute laryngeal injury 3. Initiate a randomized control trial to investigate the ability of azithromycin and budesonide to improve objective and subjective breathing measures in patients with Acute Laryngeal injury (ALgI) following endotracheal intubation.

NCT ID: NCT03031808 Recruiting - Clinical trials for Intubation Complication

Comparison of Two Induction Regimens Using Topical Lidocaine or Muscle Relaxant on Sore Throat and Hemodynamics

Start date: October 31, 2017
Phase: Phase 4
Study type: Interventional

When a surgical procedure is performed under general anesthesia, the Airways are often secured With an endotracheal tube. Some patients experience sore throat thereafter. Studies have shown a reduction of these side effects when by use of muscle relaxants or a lidocain spray prior to the intubation. At Ostfold Hospital Trust, the investigators use one of the two methods or nothing. These methods will be studied systematically. Heart rate and blood pressure rise during the intubation procedure. The investigators will also study the differences between the groups.

NCT ID: NCT02842190 Recruiting - PreTerm Birth Clinical Trials

NIPPV Versus Bi-level Nasal Continuous Positive Airway Pressure Following Extubation

Start date: January 15, 2016
Phase: N/A
Study type: Interventional

Mechanical ventilation is important in the care of preterm infants with respiratory failure, but may be associated with lung injury. Efforts are needed to avoid or minimize the use of mechanical ventilation. However, there is no consensus on the best non-invasive ventilation mode after extubation in preterm infants. Objective: To compare the effectiveness of nasal intermittent positive pressure ventilation (NIPPV) versus bi-level nasal continuous positive airway pressure (BIPAP) following extubation in preterm infants ≤ 1250 g birthweight.

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: NCT01768377 Recruiting - Clinical trials for Intubation Complication

Comparison of Intubation With Nerve Block and With Sedation in Awake Patients

Start date: November 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare intubation with nerve block with intubation with sedation in awake patients in terms of efficacy, ease, and the rate of complications and physician satisfaction