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Pulmonary Atelectasis clinical trials

View clinical trials related to Pulmonary Atelectasis.

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NCT ID: NCT02873000 Not yet recruiting - COPD Clinical Trials

Incentive Spirometry in Non-critically Ill Hospitalized Patients With Acute Respiratory Failure

Start date: April 2017
Phase: N/A
Study type: Interventional

To evaluate the use of Incentive Spirometry in Non-critically Ill Hospitalized Patients With Shortness of Breath.

NCT ID: NCT02871258 Completed - Atelectasis Clinical Trials

MetaNeb® Chest X-ray Study

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

To study objective is to evaluate the impact of use of The MetaNeb® System in clearance of atelectasis, as demonstrated by improvement in chest x-rays. This is a a non-randomized open label study, with all subjects receiving treatment with The MetaNeb® System. Subjects who qualify for enrollment in the study will receive therapy with The MetaNeb® System following the labeled instructions for the device. Details of the treatment including duration and frequency will be defined in treatment procedures.

NCT ID: NCT02870842 Completed - Clinical trials for Pulmonary Atelectasis

Fraction of Inspired Oxygen and Atelectasis in Children

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

Investigators hypothesized that maintaining low fraction of inspired oxygen would be beneficial to prevent anesthesia-induced atelectasis in mechanically ventilated children undergoing general anesthesia.

NCT ID: NCT02824146 Completed - Atelectasis Clinical Trials

Lung Recruitment Assessment With Lung Ultrasound In Pediatric Patient Scheduled For Laparoscopic Surgery

Start date: August 2014
Phase: N/A
Study type: Interventional

Anesthesia-induced atelectasis is a well-known entity observed in approximately 68-100% of pediatric patients undergoing general anesthesia. The collapse of dependent lung zones starts with anesthesia induction but can persist for hours or even days after surgery. Such anesthesia-related atelectasis has a number of negative clinical consequences such as the impairment of arterial blood oxygenation and lung mechanics as well as the predisposition for ventilator-associated lung injury. The adjustment of ventilator settings for preventing the occurrence of atelectasis and for reducing pulmonary complications remains controversial. Lung sonography (LUS) plays an important role in diagnosing pulmonary diseases in children, including atelectasis of different origins. LUS has demonstrated its high sensitivity and specificity for diagnosing anesthesia-induced atelectasis in children.

NCT ID: NCT02798133 Completed - Lung Collapse Clinical Trials

Open Lung Approach Versus Standard Protective Strategies

Start date: July 2014
Phase: N/A
Study type: Interventional

The aim of this study was to compare the effects of adding a recruitment maneuver (RM) to low tidal volume (VT) ventilation, with or without an individualized post-RM positive end-expiratory pressure (PEEP) setting in lung-healthy patients during anesthesia.

NCT ID: NCT02779595 Completed - Clinical trials for Respiratory Insufficiency

Change of Regional Ventilation During Spontaneous Breathing After Lung Surgery

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

Perioperative changes in regional ventilation by pulmonary electrical impedance tomography and spirometry will be investigated in patients at risk for postoperative pulmonary complications. Those patients undergo lung and flail chest surgery.

NCT ID: NCT02768350 Completed - Atelectasis Clinical Trials

Efficacy and Ventilatory Responses to VHI in Atelectasis Patients

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

The purpose of this study include (1) To investigate the efficacy of ventilator hyperinflation technique to re-expand lung atelectasis on patients with critical trauma who intubated and mechanical ventilation in the intensive care unit, (2) To investigate the effectiveness of ventilator hyperinflation technique to improve airway clearance on patients with critical trauma in the intensive care unit, and (3) To explore the acute responses of ventilatory functions to ventilator hyperinflation technique on patients with critical trauma who intubated and mechanical ventilation in the intensive care unit.

NCT ID: NCT02739854 Completed - Clinical trials for Pulmonary Atelectasis

Prevalence of Atelectasis in Critical Trauma Patients

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

The purpose of this study is to identify the prevalence rate and risk factors for pulmonary complications in patients with critical trauma who intubated and mechanical ventilation.

NCT ID: NCT02678559 Completed - Clinical trials for Coronary Artery Disease

Preload Dependency Evaluation With Stroke Volume Variation During Alveolar Recruitment Manoeuvres

PreDeARM
Start date: February 2016
Phase: N/A
Study type: Interventional

The principal aim is to assess impact of alveolar recruitment manoeuvres (ARM) on stroke volume variation, evaluated by trans-oesophageal echocardiography (TEE). These variations will be measured on preload dependency or preload independency status. The principal purpose is to determine if variations of stroke volume during standardized ARM can predict the preload dependency status.

NCT ID: NCT02627742 Completed - Atelectasis Clinical Trials

Evaluation of The MetaNeb® System to Reduce Postoperative Pulmonary Complications

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

To determine if a therapy regimen including treatment with The MetaNeb® System had a positive impact on the rate of pulmonary complications related to atelectasis and/or secretion retention that occur in high risk post-operative patients. This is a non-randomized facility (or hospital) level pre-post intervention study.