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Tracheal Intubation Morbidity clinical trials

View clinical trials related to Tracheal Intubation Morbidity.

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NCT ID: NCT05780385 Recruiting - Critical Care Clinical Trials

Nasotracheal Intubation in Critically Ill.

NaTra-P
Start date: February 10, 2023
Phase: N/A
Study type: Interventional

The aim of this prospective randomized trail is to compare nasotracheal versus orotracheal intubation in critically ill patients. We aim to study: - required sedation depth - rate of spontaneous breathing - extend and possibility of physiotherapy - vasopressor and sedative drug doses Participants are randomized 1:1 to receive either nasotracheal or orotracheal intubation.

NCT ID: NCT05542823 Recruiting - Clinical trials for Laparoscopic Surgery

Effect of Cuff Pressure of Endotracheal Tube on POST

Start date: October 4, 2022
Phase:
Study type: Observational

The main objective of this study is to evaluate the association between the duration of intraoperative cuff overpressure and the development of postoperative sore throat.

NCT ID: NCT05451953 Recruiting - Clinical trials for Tracheal Intubation Morbidity

Providing Oxygen During Intubation in the NICU Trial

POINT
Start date: July 21, 2022
Phase: N/A
Study type: Interventional

Tracheal intubation in the NICU is frequently complicated by severe oxygen desaturation. Apneic oxygenation, a method of applying free flowing oxygen via nasal cannula to apneic patients undergoing intubation, prevents or delays oxygen desaturation during intubation in adults and older children. We propose to enroll patients at two sites (Hospital of the University of Pennsylvania and Children's Hospital of Philadelphia) in a randomized trial in infants undergoing intubation in the NICU to determine if apneic oxygenation, compared with no respiratory support or oxygen during laryngoscopy and intubation attempts (standard care), reduces the magnitude of oxygen desaturation during tracheal intubation encounters.

NCT ID: NCT05173220 Recruiting - Clinical trials for Tracheal Intubation Morbidity

Impact of the Bougie on the Prehospital Setting Intubation Quality.

SMURIDS2
Start date: May 20, 2021
Phase:
Study type: Observational

Tracheal intubation in an out-of-hospital setting is a frequent and potentially difficult procedure. The risk of adverse events increases dramatically with the number of attempts. The failure rate of the first intubation attempt ranges from 5 to 32% and the risk factors are unclear. In recent study, the prevalence of a failed first intubation attempt was 31.4% [95% CI = 30.2-32.6] among 1546 patients managed in an out-of-hospital setting. In this multicenter study, our center (N=462) had a rate of 36% of failure of the first attempt. Seven variables were independently associated with a failed first intubation attempt. Some of the associated factors can be improved (operator training and experience), but most cannot. Moreover some of them can not be anticipated in this context. A randomized control trial performed in an emergency department and a prospective, observational, pre-post study design showed that systematic use of a bougie during the first intubation attempt improved the success rate. Our objective is to measure the impact of a modification of our intubation modalities introducing the incitation of the use of the bougie on the first intubation attempt in the prehospital setting.

NCT ID: NCT03486171 Recruiting - Emergency Medicine Clinical Trials

Tracheal Intubation and Prehospital Emergency Setting

SMURIDS
Start date: March 1, 2017
Phase:
Study type: Observational

In prehospital emergency setting, tracheal intubation is a frequent procedure (8% of interventions). Its objective is to control and protect upper airways and to optimize ventilation and oxygenation in patients with life-threatening distress. Intubation is a technical procedure which is associated with few difficulties with, in rare cases, the impossibility to do it. There are specificities of the out-of-hospital emergency with some risk factors that have been recognized in this context as well as the impossibility of assessing predictive factors of difficult intubation linked to the patient. The objective of the investigators was to describe the quality of tracheal intubation in prehospital emergency setting.

NCT ID: NCT03471884 Recruiting - Clinical trials for Non-small Cell Lung Cancer

Effects of Nonintubated Thoracoscopic Lobectomy on Lung Protection

Start date: March 2018
Phase: N/A
Study type: Interventional

A novel nonintubated thoracoscopic technique is promising to enhance recovery after thoracic surgery. However, the effects of nonintubated technique on specific organ protection in not clear yet. In this randomized trial, the effect of nonintubated technique on lung function protection will be evaluated via PaO2/FiO2 ratio, oxidative stress and inflammatory cytokines serially in lung cancer patients undergoing thoracoscopic lobectomy.

NCT ID: NCT02671877 Recruiting - Clinical trials for Tracheal Intubation Morbidity

Preoperative Fibroscopy as a Predictor of the Difficulty of Laryngoscopy and Intubation

TubeDiff
Start date: January 2016
Phase: N/A
Study type: Observational

The aim of this study is the evaluation of preoperative transnasal fiberoscopy, as a possible predictor of difficult laryngoscopy and intubation during elective general anesthesia in an adult population. Transnasal fibercoscopy is a minimally invasive examination and is routinely performed during ENT evaluation; on the other hand, current strategies used to predict the ease of intubation are still not sufficiently sensitive and specific, and an unexpected difficult or failed intubation at the induction of general anesthesia is a seriuos, and potentially fatal, emergency in anesthesia. In literature, a correlation between anatomical and functional parameters highlighted by fiberoscopy and difficulty of laryngoscopy and intubation has never been demonstrated nor indagated. If proven, this might give the Anesthestiologist further information about the expected difficulty of laryngoscopy and intubation, guiding a different - and hopefully safer - anesthesiological strategy.