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Intubation Complication clinical trials

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NCT ID: NCT03115606 Completed - Clinical trials for Intubation Complication

Comparison of C-Mac D Blade and Fastrach Laryngeal Mask Airway on Cervical Spine Motion Conditions

Start date: March 24, 2017
Phase: N/A
Study type: Interventional

In patients with cervical spine disorders or hernia, in-line stabilization and immobilization during tracheal intubation is used to avoid neck injury. With direct laryngoscopy cranio-cervical motion can result injury. The aim of the study is to compare two different device (C-Mac D blade versus fastrach LMA ) regarding cervical motions during intubation.

NCT ID: NCT03112564 Completed - Clinical trials for Intubation Complication

Endotracheal Intubation Without Muscle Relaxants

Start date: March 1, 2013
Phase: N/A
Study type: Interventional

Prospective study conducted between March 2013 and November 2014 at Hospital Universitario Puerta de Hierro-Majadahonda, in Madrid, Spain to identify complications and evaluate the efficacy of pure inhalational anesthesia induction to achieve endotracheal intubation without the use of muscle relaxant and analgesic drugs.

NCT ID: NCT03102255 Completed - Clinical trials for Intubation Complication

The Effect of 'Sniffing Position & Nasal Tip Lifting' in Nasotracheal Intubation

Start date: August 1, 2016
Phase: N/A
Study type: Interventional

The goal of this prospective randomized study is to compare the effect of nasal tip lifting during nasotracheal intubation. The question the investigators are trying to answer is: If the nasal tip is tilted, will the E-tube be more likely to enter the lower passage during nasal intubation?

NCT ID: NCT03074968 Completed - Clinical trials for Intubation Complication

Effect of Benzydamine Hydrochloride to Postoperative Sore Throat in Pediatric Patients

Start date: March 8, 2017
Phase: Phase 4
Study type: Interventional

This study is designed to examine the effect of benzydamine hydrochloride to postoperative sore throat in pediatric patients. We will spray benzydmaine hydrochloride or normal saline at oral cavity and the tip of endotracheal tube, than compare the prevalence of postoperative sore throat using smartphone application in pediatric patients.

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: NCT03026777 Completed - Clinical trials for Acute Respiratory Failure

Preventing Cardiovascular collaPse With Administration of Fluid Resuscitation Before Endotracheal Intubation

PrePARE
Start date: January 2017
Phase: Phase 4
Study type: Interventional

Endotracheal intubation is common in the care of critically ill patients. Complications of airway management in this setting are frequently encountered and may be associated with an increased risk of death. The prevention of complications during urgent and emergent endotracheal intubation is a key focus for airway management research. Post-intubation hypotension (PIH), a common complication of endotracheal intubation in the critically ill, may be prevented by a bolus of intravenous fluid prior to the start of the procedure, but this approach has not been examined in a prospective trial. There are no randomized trials of intravenous fluid administration to prevent PIH in critically ill adults. The investigators propose a randomized trial of fluid loading to prevent PIH in critically ill adults.

NCT ID: NCT03003585 Completed - Clinical trials for Intraocular Pressure

Effects of Direct Laryngoscopic and Fiberoptic Intubation on Intraocular Pressure

Start date: December 2016
Phase: N/A
Study type: Interventional

In this study, the investigators aimed to compare the effects of direct laryngoscopic and fiberoptic endotracheal intubation on intraocular pressure.

NCT ID: NCT02969889 Completed - Clinical trials for Intubation Complication

Intubation in Morbidly Obese: a Comparison of Airtraq and ILMA

Start date: June 2016
Phase: N/A
Study type: Interventional

bmı > 35 morbidly obese patients requiring endotracheal intubation enrolled in this trial. Divided into two groups Airtraq and ILMA. their effectiveness is evaluated.

NCT ID: NCT02918526 Not yet recruiting - Clinical trials for Hemodynamic Instability

Hemodynamic Study With PRAM of the Cardiovascular Response to the Positioning of the Extraglottic Device

Start date: October 2016
Phase: N/A
Study type: Interventional

The purpose of the study will be to record the hemodynamic response measured by traditional methods (non-invasive blood pressure and ECG) and Pressure Recording Analytical Method in patients undergoing laryngeal mask placement compared with the hemodynamic response measured in patients undergoing laryngoscopy and tracheal intubation for performing surgery in gynecological area and assess the differences with the two methods.

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.