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Airway Management clinical trials

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NCT ID: NCT03991325 Completed - Airway Management Clinical Trials

Sonographic Evaluation to Predict Difficult Airway Management

US airway
Start date: March 1, 2019
Phase:
Study type: Observational

the aim of this study was to evaluate the accuracy of different ultrasonographic parameters and clinical tests to predict difficult airway assessment. Ultrasonographic parameters were: hyo-mental distence, tongue width, skin to epiglottis distence and skin to hyoid bone distence. these parameters were recorded and their predictive acurracy was studied.

NCT ID: NCT03976726 Completed - Airway Management Clinical Trials

Temperature Dependent Changes in I-gel Masks

Start date: April 1, 2019
Phase:
Study type: Observational

The i-gel® mask is a second generation, single use supraglottic airway device which does not have an inflatable cuff. The cuff consists of a thermoplastic elastomer and its mechanism of sealing still remains unclear. Various theories such as temperature-dependent changes in hardness and volume expansion as well as fluid absorption have been discussed.

NCT ID: NCT03967769 Recruiting - Clinical trials for Surgical Procedure, Unspecified

Apneic Oxygénation by Nasal Canula During Infants Airway Management Study

Oxyeno
Start date: August 5, 2019
Phase: N/A
Study type: Interventional

This is a randomized clinical trial investigating the utility of apneic oxygenation via high flow nasal cannulae during airway management for infants general anaesthesia. Three groups will be compared, a control group at 0 L/min, a 0,2L/Kg/min and a 1L/Kg/min group. The primary outcome will be the time (in seconds) between onset of apnea and one of theses end-points : desaturation (SPO2 <95%) or Airway management completed.

NCT ID: NCT03942809 Completed - Airway Management Clinical Trials

Clinical Evaluation of the Revised iLTS-D2

iLTS-D2
Start date: August 13, 2019
Phase: N/A
Study type: Interventional

A interventional, non-randomized, controlled study to evaluate the revised iLTS-D2 in anesthetized patients.

NCT ID: NCT03908411 Completed - Airway Management Clinical Trials

The Effect of Paratracheal Pressure on the Glottic View

Start date: September 5, 2019
Phase: N/A
Study type: Interventional

Paratracheal pressure may have a role in the prevention of pulmonary aspiration. The effects of paratracheal pressure on glottic view, ease of facemask ventilation, or tracheal intubation are not studied yet. In this study, the subjects are divided into two groups (group I: paratracheal pressure applied during induction of anesthesia, group II: conventional Sellick's maneuver applied during induction of anesthesia). Investigators will assess the glottic view during direct laryngoscopy.

NCT ID: NCT03856073 Not yet recruiting - Education Clinical Trials

The Training and Evaluate Effect on Clinical Airway Management for Novices.

Start date: March 6, 2019
Phase: N/A
Study type: Interventional

In this self-control experiment, anesthesiologists without experiment of bronchoscopy working in anesthesiology department in Peking Union Medical College Hospital will receive a training and evaluation procedure in simulation and clinical practice about clinical airway management. The objects was (1) to investigate the improvements of manufacturing bronchoscopy in simulation and clinical practice before and after training on simulation, (2) to record the study curve and efforts trainees needed to achieve proficiency and self-confidence on simulation, (3) to record the curve of manufacturing from skilled to unskilled, (4)to evaluate if status manufacturing on simulations could reflect the ones in clinical practice.

NCT ID: NCT03854760 Not yet recruiting - Education Clinical Trials

The Training and Evaluate Effect on Clinical Airway Management

Start date: March 5, 2019
Phase: N/A
Study type: Interventional

In this self-control experiment, anesthesiologists with limited experiments of bronchoscopy working in anesthesiology department in Peking Union Medical College Hospital will receive a training and evaluation procedure in simulation and clinical practice about clinical airway management. The objects was (1) to investigate the improvements of manufacturing bronchoscopy in simulation and clinical practise before and after training on simulation,(2) to record the efforts trainees needed to achieve experienced on simulation, (3) to evaluate if status manufacturing on simulations could reflect the ones in clinical practise.

NCT ID: NCT03848559 Completed - Airway Management Clinical Trials

Airway Management With Simulated Microgravity Using a Submerged Model

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

Trained anesthesiologist- or emergency physician-divers will perform an airway management in simulated microgravity on a submerged model.

NCT ID: NCT03845998 Completed - Airway Management Clinical Trials

Compare the Efficacy of Different Laryngeal Mask Size Selection Methods in General Anesthesia in Children

Start date: February 25, 2019
Phase: N/A
Study type: Interventional

The laryngeal mask is widely used in general anesthesia in children. Selection of an appropriately sized laryngeal mask airway (LMA) is critical to ensure safe and effective use of the device. In children, the appropriate size of the LMA to be used is usually determined by the patient's weight. Up to now, this is the gold standard method, but the weight-related technique is not always possible. The patient's weight is sometimes unknown or medical staff do not remember the relationship between weight and size. Moreover, there are no constant correlations between laryngeal airways and body indices such as height and weight, so that the standard method could cause an inappropriate size of laryngeal mask airway to be chosen. Researchers from Spain introduced a new technique to determine the size of the LMA in children by choosing the LMA that best matched the combined widths of the patient's index, middle and ring fingers, but needs to be formally evaluated in clinical application. In order to compare the application effects of two methods (weight-related and three-fingers), we designed a research plan.

NCT ID: NCT03687424 Not yet recruiting - Obesity Clinical Trials

Can High-flow Nasal Oxygenation Improve Oxygen Saturation During Analgo-sedation in Obese Adults?

Start date: October 30, 2018
Phase: N/A
Study type: Interventional

Obesity is omnipresent problem in everyday anesthesiology practice associated with low level of blood oxygen (hypoxemia) during analgo-sedation. Overweight outpatients are often scheduled for colonoscopy usually undergo analgo-sedation. In obese patients, intravenous analgo-sedation often diminish respiratory drive causing hypoxemia. To avoid hypoxemia, low-flow nasal oxygenation (LFNO) of 2-6 L/min is applied via standard nasal catheter to provide maximum 40 % of inspired fraction of oxygen (FiO2). LFNO comprises applying cold and dry oxygen which causes discomfort to nasal mucosa of patient. LFNO is often insufficient to provide satisfying oxygenation. Insufficient oxygenation adds to circulatory instability - heart rate (HR) and blood pressure (BP) disorder. On the other side, high-flow nasal oxygenation (HFNO) brings 20 to 70 L/min of heated and humidified of O2/air mixture up to 100% FiO2 via specially designed nasal cannula. Heated and humidified O2/air mixture is much more agreeable to patient. HFNO brings noninvasive support to patients' spontaneous breathing by producing continuous positive pressure of 3-7 cmH2O in upper airways consequently enhancing oxygenation. Investigators intend to analyze effect of HFNO vs. LFNO on oxygen saturation during procedural analgo-sedation for colonoscopy in obese adult patients. Investigators expect that obese patients with preserved spontaneous breathing, oxygenized by HFNO vs. LFNO, will be less prone to hypoxemia thus more respiratory and circulatory stable during procedural analgo-sedation for colonoscopy. Obese patients with applied HFNO should longer preserve: normal oxygen saturation, normal level of CO2 and O2, reflecting better respiratory stability. Investigators expect obese participnts to have more stable HR and BP, reflecting improved circulatory stability. There will be less interruption of breathing pattern of obese patients and less necessity for attending anesthesiologist to intervene.