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Pulmonary Atelectasis clinical trials

View clinical trials related to Pulmonary Atelectasis.

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NCT ID: NCT03614091 Recruiting - Pain, Postoperative Clinical Trials

Paravertebral Block Versus Erector Spinae Plane Block for Modified Radical Mastectomy in Womens.

Start date: February 1, 2020
Phase: N/A
Study type: Interventional

postoperative pain following Modified radical mastectomy is severe specially after dissection of tissues .paravertebral plane block provides an excellent postoperative analgesia for women's,but it carry the risk of pneumothorax which it reported in some cases.Erector spinae plane block is a recent block has been mentioned in many case reports as a safe,quick and can be used in outpatient setting. we use a comparative study to compare the postoperative analgesia between both blocks and the affection of postoperative pain following both blocks if any on pulmonary functions.

NCT ID: NCT03469323 Recruiting - Atelectasis Clinical Trials

Effects of Succinylcholine on Nonintubated Thoracoscopic Surgery

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

A safe and effective surgical environment is important for nonintubated thoracoscopic surgery. The investigators hypothesize that mini-dose succinylcholine can induce ultra-short period of apnea, by which the ventilatory responses to open pneumothorax were abolished and may facilitate rapid and satisfying collapse of the operated lung during nonintubated thoracoscopic surgery.

NCT ID: NCT03369483 Recruiting - Lung Collapse Clinical Trials

Abdominal Pressure Assessment Following Open Abdominal Surgery

AbdoPress
Start date: March 13, 2018
Phase:
Study type: Observational

During abdominal surgery, the intra abdominal pressure may increase determining lung bibasal atelectasis. The investigators hypothesized that the application of Positive End Expiratory Pressure (PEEP) promptly after extubation through Continuous Positive Airway Pressure (CPAP) would improved gas exchange, especially in those patients with abdominal pressure values close to those applied by CPAP. The investigators have therefore designed this subset study enrolling patients randomized to receive CPAP in the "Prevention of Respiratory Insufficiency after Surgical Management (PRISM)" Trial in order to ascertain the abdominal pressure in post-surgical patients (abdominal open surgery procedures) enrolled in PRISM trial. In addition they would evaluate the effects of CPAP on abdominal pressure and consequently on arterial blood gas, and whether there is a correlation between PEEP values, abdominal pressure values and arterial blood gas. One hundred patients included in CPAP group of the PRISM trial will be enrolled in this subset study. The investigators will perform measurements of the abdominal pressure an urinary catheter connected with an intra-abdominal pressure device (Uno-Meter ® - Uno-medical) in all patients undergoing on open-surgical procedures after mechanical ventilation withdrawal and extubation, 30 minutes and 4 hours after the application of CPAP.

NCT ID: NCT03311347 Recruiting - Clinical trials for Pulmonary Atelectasis

Atelectasis Formation: Role of Positive Pressure Breathing, Hyperoxia, and Hypobaria

Start date: September 14, 2015
Phase: N/A
Study type: Interventional

The primary aim of this project is to get further knowledge of the physiology of flight atelectasis and its prevention. We seek to: 1) assess whether low levels of positive pressure breathing can prevent atelectasis formation in humans during exposure to hyperoxia and +Gz-accelerations. 2) get further knowledge on the effects of hypobaria on regional ventilation and perfusion. A secondary aim is to evaluate the effect of anti G-trouser inflation on ventilation and regional perfusion.

NCT ID: NCT03133754 Recruiting - Lung Collapse Clinical Trials

OLA to Lowest DP in Cardiac Surgery

Start date: July 10, 2017
Phase: N/A
Study type: Interventional

This study aims to compared the effects in driving pressure of an open-lung strategy with a positive end-expiratory pressure (PEEP) titrated to best driving pressure (DP) after a RM versus the recommended protective PEEP of 5 cmH2O without a recruitment manuever in non-obese patients undergoing cardiac surgery.

NCT ID: NCT03112811 Recruiting - Atelectasis Clinical Trials

Influence of Techniques of Chest Physiotherapy in the Pediatric Intensive Care

Start date: April 3, 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of the autogenic drainage and the intrapulmonary percussive ventilation on the levying of the lung atelectasis, by means of the thoracic imaging (thoracic ultrasound and radiography), at the intubated or extubated child with the ventilatory support.

NCT ID: NCT03019354 Recruiting - General Anesthesia Clinical Trials

The Effect of Using High-flow Nasal Oxygen-delivery System in Patients Under Intravenous General Anesthesia

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

In general anesthesia, gas exchange was altered by shunt and uneven ventilation perfusion ratios. Lung atelectasis was a cause of impaired oxygenation. High-flow nasal cannula oxygen therapy delivers adequately heated and humidified medical gas at up to 60 L/min of flow. It has physiological effects: reduction of anatomical dead space, positive end expiratory pressure (PEEP) effect, constant fraction of inspired oxygen, and good humidification. The hypothesis of this study is using high-flow nasal oxygen in intravenous general anesthesia could improve lung function and prevent lung atelectasis.

NCT ID: NCT02431455 Recruiting - Pneumonia Clinical Trials

The Effect of Postoperative Incentive Spirometry on Pulmonary Function and Pulmonary Complications in Bariatric Surgery

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

This study evaluates the omission of incentive spirometry use following bariatric surgery. Half of participants will receive an incentive spirometer while the other half will not. Oxygen saturation and pulmonary complications after surgery will be measured to examine the effectiveness of incentive spirometry.

NCT ID: NCT02314845 Recruiting - Clinical trials for Pulmonary Atelectasis

Optimizing Intraoperative Mechanical Ventilation Using EIT-titrated PEEP

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

The purpose of this randomized single center study is to determine the individual PEEP value that produces the best possible compromise of lung collapse and lung hyperdistention. Patients submitted to general anesthesia and mechanical ventilation during surgery (laparoscopy and open surgery) will participate. A PEEP titration procedure will be performed and the "optimal PEEP" value will be determined by electrical impedance tomography (EIT). An ultrasound will be used to record each step of the PEEP titration procedure in a sub-sample of patients. A total of 40 patients will be mechanically ventilated using physiological tidal volume (TV=6mL/kg of IBW) and fraction of inspired oxygen (FIO2) of 0.5 and will be randomized to one of two groups: "optimal PEEP" or a "low PEEP" (4cmH2O). Lung collapse and mechanics will be monitored by EIT throughout the intraoperative period. After extubation, a lung CT will be performed to evaluate the amount of lung collapse.

NCT ID: NCT02285894 Recruiting - Atelectasis Clinical Trials

Can 10 Seconds Inspiratory Hold Open Atelectasis in Mechanically Ventilated Patients?

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

This study evaluates whether sustaining inspiratory pressure for 10 seconds at a time can open collapsed lung areas in non-dependant regions of the lung in mechanically ventilated patients.