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Pulmonary Atelectasis clinical trials

View clinical trials related to Pulmonary Atelectasis.

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NCT ID: NCT03962725 Terminated - Respiratory Failure Clinical Trials

Avoiding Neuromuscular Blockers to Reduce Complications

Start date: August 7, 2019
Phase: Phase 4
Study type: Interventional

The goal of this study to evaluate whether eliminating the use of non-depolarizing neuromuscular blocking agents (NMBA) for maintenance of general anesthesia reduces postoperative pulmonary complications in higher risk patients.

NCT ID: NCT03943433 Completed - Clinical trials for Atelectasis, Postoperative Pulmonary

Oxygen Concentration During Alveolar Recruitment

Start date: May 15, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of oxygen concentration during alveolar recruitment on absorption ateletasis.

NCT ID: NCT03856918 Completed - Clinical trials for Video-assisted Thoracic Surgery

Optimal Level of PEEP in Protective One-lung Ventilation

Start date: May 28, 2019
Phase: N/A
Study type: Interventional

Protective ventilation strategy has been widely applied in the field of thoracic surgery requiring one-lung ventilation to reduce postoperative pulmonary complications. Low tidal volume, positive end-expiratory pressure (PEEP), and intermittent recruitment maneuver are key components of protective ventilation strategy. Recent evidence suggests that a tidal volume of 4-5 ml/kg should be applied during protective one-lung ventilation. However, optimal level of PEEP is still unclear. This study aims to investigate optimal level of PEEP to minimize postoperative atelectasis by comparing modified lung ultrasound score in patients applied protective one-lung ventilation using PEEP of 3, 6, or 9 cm of water during thoracic surgery.

NCT ID: NCT03828513 Active, not recruiting - Clinical trials for Bariatric Surgery Candidate

Can the Effects of High Flow Nasal Cannula Oxygenation on Postoperative Atelectasis be Evaluated With Lung Ultrasound

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

Evaluate the effects of high-flow nasal oxygen therapy on atelectasis in the perioperative period by lung ultrasound (LUS) in bariatric surgery patients.

NCT ID: NCT03817177 Recruiting - Atelectasis Clinical Trials

Application of High Flow Nasal Cannula for Prevention of Post-extubation Atelectasis in Children Undergoing Surgery

Start date: March 2, 2019
Phase: N/A
Study type: Interventional

postoperative atelectasis observation by ultrasound after application of high flow nasal cannula oxygenation

NCT ID: NCT03763461 Completed - Clinical trials for Pulmonary Atelectasis

HFNC During Awake Craniotomy - Impact on Patient Comfort

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

Background: Patients undergoing awake brain surgery are exposed to non-humidified, non-warmed oxygen/air mix flow through a face mask for a prolonged duration. This causes increased discomfort, inadequate breathing with the risk for hypoxia perioperatively. Humidified high flow nasal cannula (HFNC) oxygen therapy potentially improves patient comfort, oxygen/air exchange, improves surgical conditions and prevents atelectasis of the lung, compared to traditional oxygen administration using a face mask in patients undergoing awake brain surgery. Results of this trial will be used to initiate a more extensive, multicenter trial to further characterize the potential impact of HFNC.

NCT ID: NCT03739697 Completed - Atelectasis Clinical Trials

Effect of Spontaneous Breathing on Atelectasis During Induction of General Anesthesia in Patients in Infants

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

spontaneous breathing on occurrence of atelectsis in infants

NCT ID: NCT03694665 Completed - Atelectasis Clinical Trials

Monitoring Lung Recruitment Maneuver in Anesthetized Morbidly Obese

Start date: September 11, 2016
Phase: N/A
Study type: Interventional

Morbid obese patients present changes in respiratory physiology caused by weight overload. Intraoperative atelectasis is a pulmonary complication that affects not only gas exchange but also respiratory mechanics. The present study was aimed to test the role of different parameters for monitoring the treatment of atelectasis by a lung recruitment maneuver.

NCT ID: NCT03686631 Completed - Clinical trials for Post-Op Complication

The Digital Incentive Spirometer (DIS): Improving Adherence to Incentive Spirometry

DIS
Start date: July 9, 2019
Phase: N/A
Study type: Interventional

The purpose of the protocol is to assess how incentive spirometer data gathered via a smartphone platform can be utilized to improve participant adherence to prescribed incentive spirometer exercises in the post-operative period. Half of the participants will receive a standard of care incentive spirometer with a passive tracking device while the other half of the participants will receive a smartphone connected device and smartphone with an application that will encourage their use.

NCT ID: NCT03630484 Completed - Clinical trials for Pulmonary Atelectasis

Ventilator Hyperinflation and Manual Rib Cage Compression

Start date: November 28, 2014
Phase: N/A
Study type: Interventional

This is a randomized crossover trial to evaluate the effects of thoracic compression applied alone or in association with hyperinflation maneuver with the ventilator. In addition, the mobilized volume and peak expiratory flow resulting from both maneuvers will be evaluated.