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Atelectasis clinical trials

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NCT ID: NCT01858844 Completed - Atelectasis Clinical Trials

Chest Compression Technique in Infants

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

Evaluate the effect of chest manual compression technique (CCT) in the variables of oxygenation, hemodynamic and respiratory work in infants with respiratory diseases that are associated with atelectasis.

NCT ID: NCT01826968 Completed - Pneumonia Clinical Trials

Alveolar Recruitment Maneuver During Cesarean Section Improves Lung Compliance

CSRecGHPyr
Start date: January 2013
Phase: Phase 2
Study type: Interventional

The investigators tested the hypothesis that alveolar recruitment maneuver during cesarean section and in women under general anesthesia improves lung compliance and gas exchange. The investigators applied recruitment maneuver and positive end expiratory pressure (PEEP) 8 cmH2O. The maximum alveolar pressure limit (Ppeak)was 45 cmH2O during the recruitment maneuver. The primary end point of the study is the improvement of the lung compliance measured as volume difference/pressure difference (dv/dp) or ml/cmH2O

NCT ID: NCT01810172 Completed - Atelectasis Clinical Trials

Digital Air Leak Monitoring for Patients Undergoing Lung Resection

Start date: April 2013
Phase: N/A
Study type: Interventional

Often the decision for chest tube removal or trial of chest tube clamping is based on subjective assessment. This can lead to delay in chest tube removal. Recently, monitoring and recording of air leaks has been done using digital pleural drainage devices. This provides us with objective and continuous recording of air leaks as well as changes in pleural pressure. Our hypothesis is that the use of the ATMOS digital pleural drainage system will result in shorter hospital stay in comparison to traditional pleural drainage systems.

NCT ID: NCT01749436 Completed - Atelectasis Clinical Trials

Role of Lung Ultrasound Imaging for Intraoperative Monitoring of Atelectasis During Laparoscopic Surgery

Start date: April 2013
Phase: N/A
Study type: Observational

General anesthesia results in the development of atelectasis in the dependent areas of the lungs exposing patients to an increased risk of hypoxemia. During laparoscopic procedures, pneumoperitoneum increases already present atelectasis. Several methods have been suggested to reduce the impact of atelectasis during surgery. However, few intraoperative modalities for the diagnosis and monitoring of atelectasis are available. Lung ultrasound imaging is a promising non-invasive, non-radiant, portable and easy to use tool that as yet to be studied in the intraoperative setting. This observational study will aim to clarify the role of lung ultrasound imaging during laparoscopic surgery for the diagnostic and monitoring of atelectasis. This study is designed to: - Demonstrate a link between the lung ultrasound aeration score, the partial pressure of oxygen in arterial blood (PaO2) / fraction of inspired oxygen (FiO2) ratio and the oxygenation index. - In the event of intraoperative desaturation, study the impact of positive end-expiratory pressure (PEEP) and/or increase of FiO2 on the aeration score. - Study the impact of pain on diaphragmatic function and the aeration score. Our hypothesis is that lung ultrasound imaging allows detection of lung aeration changes associated with induction of general anesthesia, pneumoperitoneum, emergence from anesthesia and changes occurring during the stay in the recovery room.

NCT ID: NCT01416519 Completed - Pneumonia Clinical Trials

Physiotherapy Technique Decreases Respiratory Complications After Cardiac Operation

Start date: September 2011
Phase: N/A
Study type: Interventional

The objective of this study is to assess whether there is a difference between a care protocol with the use of incentive spirometry (Voldyne ®) and another with the application of NIV (non invasive ventilation with single-level pressure) as a form of therapy. The main focus of the study is to determine the incidence of pulmonary complications in each technique.

NCT ID: NCT01095276 Completed - Atelectasis Clinical Trials

Impact of Nebulized Dornase Alpha on Mechanically Ventilated Patients

Start date: November 2005
Phase: N/A
Study type: Interventional

The investigators hypothesized that dornase alpha, administered twice a day (BID) by in-line nebulizer, would improve oxygenation, compliance, and time to extubation in adult patients receiving mechanical ventilation.

NCT ID: NCT01073917 Completed - Atelectasis Clinical Trials

Effects of Spontaneous Breathing Activity on Atelectasis Formation During General Anaesthesia

SBAFGA
Start date: March 2010
Phase: N/A
Study type: Interventional

Atelectasis and redistribution of ventilation towards non-dependent lung zones are a common side effects of general anesthesia. Spontaneous breathing activity (SBA) during mechanical ventilation may avoid or reduce atelectasis, improving arterial oxygenation; however, it is unclear whether these effects play a significant role during general anesthesia in patients with healthy lungs. Earlier studies on ventilation during general anesthesia had to rely on computed tomography (CT) findings. Recent advances in lung imaging technology allow to assess the regional aeration of the lungs continuously and non-invasive by electrical impedance technology (EIT). In this work, we will use the EIT to assess ventilation changes from the time before induction of anesthesia until discharge from the post-anesthesia care unit. Our main focus is the difference caused by pure positive pressure ventilation (PCV) and assisted spontaneous breathing (pressure support ventilation, PSV). Our findings would improve our understanding of the physiology of the lungs during general anesthesia and would help to improve the standards of respiratory care during anesthesia

NCT ID: NCT00715741 Completed - Atelectasis Clinical Trials

Does High Intraoperative Inspired Oxygen Reduce Postoperative Arterial Oxygen Saturation?

Start date: June 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether breathing high levels of oxygen during surgery affects oxygen levels after surgery. The second purpose of this study is to determine whether giving positive end expiratory pressure PEEP and high oxygen together affects patients oxygen levels after surgery.

NCT ID: NCT00671723 Completed - Atelectasis Clinical Trials

Dornase Alpha Versus Hypertonic Saline for Lung Atelectasis in Non-Cystic Fibrosis Patients

Start date: October 2006
Phase: N/A
Study type: Interventional

Despite the lack of trials proving the efficacy of DNase in non cystic fibrosis patients, it is currently heavily used in this population. In fact, per evidence of barcode scanning via Meditech computer system at OU Medical Center 93% of the DNase prescribed in 2005 was for non Cystic fibrosis patients with an estimated yearly cost of $341,968.15.In vitro studies showed that the effect of Dnase was minimal on sputum viscosity when compared to Hypertonic saline . Furthermore recent studies on hypertonic saline in cystic fibrosis patients showed that it is an inexpensive and safe therapy when preceded by a bronchodilator in patients with cystic fibrosis. We hereby propose a prospective randomized trial to compare the efficacy of hypertonic saline, DNase, vs. normal saline in the treatment of atelectasis in non cystic fibrosis, mechanically ventilated patient.

NCT ID: NCT00665405 Completed - Cesarean Section Clinical Trials

Atelectasis During Delivery - Comparing Cesarian (c) -Section and Labor

Start date: July 2006
Phase: N/A
Study type: Observational

Pregnancy promotes respiratory system's restrictive component. This study observes the generation of atelectasis during labor.