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Upper Airway Obstruction clinical trials

View clinical trials related to Upper Airway Obstruction.

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NCT ID: NCT05328206 Recruiting - Clinical trials for Respiratory Distress

Air Leak Test In Pediatric Intensive Care Unit

ALTIPICU
Start date: October 5, 2022
Phase:
Study type: Observational

Respiratory distress by upper airway obstruction (UAO) is the primary etiology of extubation failure in children hospitalized in pediatric intensive care unit (PICU). This complication may require various invasive therapeutic which increase morbi-mortality and length of hospital stay. Cuff leak test (CLT) measured prior extubation to predict post-extubation UAO has been widely used in adult. The test compared expired tidal volume with cuff inflated and cuff deflated in order to predict UAO. Despite its frequent use in PICU, his predictive value to predict UAO in children is still poorly documented. Therefore, we conducted the first multicentric, prospective study to evaluate the CLT as a predictor of post-extubation UAO in critically ill children. The Primary objective is to assess the effectiveness of CLT in predicting severe respiratory distress by UAO within 48 hours of extubation in a critically ill children.

NCT ID: NCT04419883 Completed - Clinical trials for Upper Airway Obstruction

A New Flexible Extended-Length Pharyngeal Airway for Deep Sedation

Start date: March 5, 2019
Phase:
Study type: Observational

The purpose of this prospective pilot provider adoption study was to evaluate user experience a new airway device in adult patients with airway obstruction under deep sedation. Fifteen hospital systems served as testing sites. Fifty-four anaesthetist providers reported their experience with the airway device in 84 cases across two phases of surveying.

NCT ID: NCT03467880 Recruiting - Asthma Clinical Trials

Multicenter Study of Impulse Oscillometry in Chinese

Start date: September 2016
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to establish the reference values of impulse oscillometry (IOS) in healthy Chinese, and compare the indices of IOS in patients with lung disease, such as chronic obstructive pulmonary disease (COPD), asthma, interstitial lung disease (ILD), and upper airway Obstruction (UAO).

NCT ID: NCT03138850 Completed - Apnea, Obstructive Clinical Trials

Improve Oxygenation and Capnographic Detection During Sedative EGD

Start date: May 3, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of mandibular advancement bite block and high flow nasal cannula to standard bite block for oxygenation, capnographic measurement, prevention of hypoxemia, intervention events and adverse effects during endoscopic examinations.

NCT ID: NCT02683772 Completed - Respiratory Failure Clinical Trials

Astral VAPS AutoEPAP Clinical Trial

Start date: April 15, 2016
Phase: Phase 3
Study type: Interventional

Patients with chronic respiratory failure such as those associated with Chronic Obstructive Pulmonary Disease (COPD), Obesity Hypoventilation Syndrome (OHS), Obstructive Sleep Apnea (OSA) or Neuromuscular Disease (NMD) are increasingly managed with domiciliary non-invasive positive pressure ventilation (NIPPV). The aim of this study is to now compare the Automatic Expiratory Positive Airway Pressure (AutoEPAP) algorithm with a fixed manual EPAP in iVAPS mode on an Astral mixed mode ventilator. It is proposed that the automatic settings of AutoEPAP will be as effective at managing respiratory failure and upper airway obstruction (UAO) as manual EPAP on the Astral device. Specifically demonstrating that the AutoEPAP function is as effective at treating UAO as manual EPAP.

NCT ID: NCT02613429 Completed - Clinical trials for Upper Airway Obstruction

Identification of Airway Structures Necessary for Airway Access Via the Skin

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

Literature shows that anaesthetists have a low success-rate when trying to access the airway percutaneously in case of failed ventilation and intubation. The study will investigate anaesthetists ability to locate the trachea and the thyroid cartilage and the cricoid cartilage in patients, using different methods including application of ultrasonography.

NCT ID: NCT02317042 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Juno Perth Clinical Trial

Start date: May 29, 2015
Phase: N/A
Study type: Interventional

This study is to evaluate the efficacy of a new therapy (Automatic Expiratory Positive Airway Pressure with intelligent Volume Assured Pressure Support (AutoEPAP iVAPS)) designed to treat respiratory insufficiency, respiratory failure and/or nocturnal hypoventilation with upper airway obstruction. The study will be performed in two phases: In a sleep unit and in the home environment. The new therapy will be compared against two existing ventilator therapies: "Spontaneous Timed (ST) mode" and "Intelligent Volume Assured Pressure Support (iVAPS)".

NCT ID: NCT01719224 Completed - Clinical trials for Sleep Disordered Breathing

Incidence of Sleep-disordered Breathing and Upper Airway Collapsibility in Postpartum Patients and Its Intervention

Start date: March 2012
Phase: N/A
Study type: Interventional

The investigators hypothesized that sleeping in a 45 degrees elevated body position decreases the likelihood of upper airway vulnerability to collapse early after delivery. Furthermore, the investigators want to elucidate the anatomical and physiological risk factors that contribute in the upper airway obstruction in post-partum patients.

NCT ID: NCT01651286 Completed - Clinical trials for Mechanical Ventilation Complication

Nasal Mask Ventilation During the Induction of General Anesthesia

Start date: June 2012
Phase: N/A
Study type: Interventional

Recently, the investigators demonstrated that nasal route ventilation is superior to the nasal-oral combined ventilation in the absence of jaw thrust and chin up maneuvers. The investigators hypothesize nasal mask ventilation may reduce the incidence of difficult mask ventilation during the induction of general anesthesia by: 1) producing a better seal than full face mask, and 2)establishing a greater airway patency and more effectively ventilate than full face mask ventilation. The investigators intend to test this hypothesis on adult patients during the induction of general anesthesia in the absence of muscle relaxation.

NCT ID: NCT01627925 Withdrawn - Clinical trials for Upper Airway Obstruction

Safety Study of Positive Airway Pressure Via a Nasal Mask in Obese Patients

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

Upper airway obstruction (UAO) is a frequently occurring complication during induction of general anesthesia. The American Society of Anesthesiologist (ASA) closed claim analysis of anesthesia complications indicate that a difficult airway is one of the most challenging scenarios continuously facing anesthesia providers. The mechanism of UAO during anesthesia has not been well understood. Posterior displacement of soft palate, tongue and epiglottis are believed to be the primary contributing factors. Obesity is well known to be an essential characteristic which reflects propensity to UAO. The mechanism of UAO during anesthesia shares many similarities with the upper airway obstruction observed during obstructive sleep apnea (OSA). Nasal continuous positive airway pressure (nCPAP) via nasal mask (NM) can maintain the airway patent with near 100% success in patients with OSA. Obesity is a major risk factors for obstructive sleep apnea and obese patients have a higher prevalence of UAO during anesthesia. Therefore, the investigators hypotheses that nCPAP should eliminate airway obstruction in obese patients under anesthesia. The investigators propose to test this hypothesis and determine the efficacy of nCPAP on maintaining airway patency in obese patients who require general anesthesia.