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Postoperative Atelectasis clinical trials

View clinical trials related to Postoperative Atelectasis.

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NCT ID: NCT06304493 Not yet recruiting - Clinical trials for Respiratory Insufficiency

REMINDers for Incentive Spirometry in PACU (REMIND-IS in PACU)

Start date: March 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the frequency of use of incentive spirometry during the stay in the Post-Anesthesia Care Unit (PACU) increases with visual and auditory electronic reminders, as compared to not having those reminders.

NCT ID: NCT06267443 Not yet recruiting - Postoperative Pain Clinical Trials

Erector Spina Block or Parasternal Block Plus Chest Tube Wound Infiltration for Cardiac Surgeries

Start date: March 1, 2024
Phase: N/A
Study type: Interventional

Pain management is important after coronary artery bypass graft (CABG) surgery. Intravenous morphine is the gold standard for pain relief, but its sedation, cough suppression and decreased bowel movements limit its use. Analgesia with regional methods after surgery provides effective analgesia by reducing morphine consumption. In this study we have planned to compare the erector spina plane block with parasternal block +local infiltration to chest tube areas.

NCT ID: NCT06115668 Recruiting - Clinical trials for Positive End-expiratory Pressure

Individualized Positive End-Expiratory Pressure (PEEP) on Oxygenation, Hemodynamics, and Early Postoperative Atelectasis in Laparoscopic Bariatric Surgery

Start date: November 5, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effectiveness of intraoperative individualized positive end-expiratory pressure (PEEPIND) titration, compared to fixed positive end-expiratory pressure of 5 cmH2O, on oxygenation, hemodynamic variables, and early postoperative complications in obese patients undergoing laparoscopic bariatric surgery.

NCT ID: NCT05325463 Completed - Clinical trials for Scoliosis; Adolescence

Lung Recruitment Maneuvers for Postoperative Atelectasis Prevention After Idiopathic Adolescents' Scoliosis Correction

Start date: April 10, 2022
Phase: N/A
Study type: Interventional

The investigators hypothesized that an ultrasound-guided lung recruitment maneuvers would be more effective in preventing postoperative atelectasis than conventional alveolar recruitment after surgical correction of idiopathic adolescent scoliosis.

NCT ID: NCT04258202 Completed - Atelectasis Clinical Trials

Ventilator-driven Alveolar Recruitment Maneuver

Start date: March 2, 2020
Phase: N/A
Study type: Interventional

During laparoscopic surgery, gas infiltration and head down position cause pulmonary atelectasis. Alveolar recruitment maneuvers are beneficial in reopening collapsed alveoli and improving lung mechanics. Ventilator-driven Alveolar recruitment maneuvers may restore lung volume but it remains unknown which method is most effective. The primary aim was to compare the efficacy of two ventilator-driven ARMs method using incremental tidal volume or positive end expiratory pressure(PEEP) until plateau pressure 30 cmH20 (within driving pressure 20 cmH20).

NCT ID: NCT04253834 Completed - Clinical trials for Postoperative Atelectasis

GO2 PEEP Study: Bidirectional Oxygenation Valve in Postoperative Atelectasis

Start date: August 27, 2020
Phase: N/A
Study type: Interventional

This study compares a novel breathing device, called the GO2 Mouthpiece, to the standard breathing tool called the incentive spirometer, thus improving respiratory dynamics of the postoperative patient.

NCT ID: NCT04169607 Completed - Clinical trials for Postoperative Atelectasis

Effect of Intraoperative Dynamic Compliance Guided Individualized Positive End-expiratory Pressure on Postoperative Atelectasis After Laparoscopic Bariatric Surgery

Start date: December 16, 2019
Phase: N/A
Study type: Interventional

This study intends to explore the effect of dynamic compliance guided individualized positive end-expiratory pressure titration strategy on reducing the level of postoperative atelectasis in obese patient who have laparoscopic bariatric surgery.The results of the study are to assess the effects of this intervention on the incidenceļ¼Œduration of postoperative atelectasis and other complications including hypoxemia etc. after laparoscopic bariatric surgery.And reducing the burden of postoperative atelectasis on patients and their families, hospitals and public resources.

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.