Clinical Trials Logo

Pulmonary Atelectasis clinical trials

View clinical trials related to Pulmonary Atelectasis.

Filter by:

NCT ID: NCT05647434 Recruiting - Ventilator Lung Clinical Trials

Effect of Sustained Inflations on Lung Atelectasis During Pediatric Laparoscopic Surgery

Start date: December 30, 2022
Phase: N/A
Study type: Interventional

The aim of our study is to assess the beneficial effect of sustained inflations as a recruitment manoeuvre, using LUS examinations, on the degree of lung atelectasis that occurs in pediatric patients undergoing laparoscopic surgery. Objectives - To assess the effect of general anaesthesia and capnoperitoneum on lung atelectasis in the paediatric patients by using LUS examination - To assess the effect of sustained inflations as a recruitment manoeuvre in decreasing lung atelectasis caused by general anaesthesia and capnoperitoneum by using LUS examination Hypothesis Our main hypothesis is that the use of repeated Sustained Inflation as a recruitment manoeuvre in pediatric patients undergoing laparoscopic surgery will result in decreased atelectasis compared to conventional ventilation.

NCT ID: NCT05627024 Recruiting - Atelectasis Clinical Trials

Effects of Different Inhalation Oxygen Concentrations on Postoperative Atelectasis

DIOCA
Start date: January 11, 2023
Phase: Phase 4
Study type: Interventional

This study was a single-center, prospective, randomized controlled, two-arm study. This study will be conducted in the First Hospital of China Medical University. the investigators aimed to investigate the effects of different inspired oxygen concentrations in lung protective ventilation strategies on immediate postoperative atelectasis and intraoperative changes of oxygenation index in patients undergoing neurosurgical surgery in the supine position.

NCT ID: NCT05528159 Recruiting - Atelectasis Clinical Trials

Lung Ultrasound Score (LUS) Change in Robotic and Laparoscopic Urologic Surgeries

Start date: December 7, 2022
Phase:
Study type: Observational

Robotic and laparoscopic surgeries are tend to cause lung atelectasis due to the insufflation of CO2 into abdomen. However, ultrasonographic measurement for this phenomenon and its clinical use is not well investigated. In this particular study, It is aimed to observe lung ultrasound score (LUS) changes in robotic and laparoscopic supine position surgeries such as prostatectomies and cystectomies. LUS is a pragmatic measurement method that calculates the degree of atelectasis and consolidation in the lungs. Both hemithoraxes are separated into 3 different segments with vertical lines (one between the parasternal line and anterior axillary line, one between the anterior and posterior axillary line, and one posterior to the posterior axillary line). These vertical segments are also divided into two with an horizontal line on the nipple. Lung ultrasonography is applied in all 12 zones for both lungs in the intercostal regions and a scoring system is used. Accordingly, pure A lines (transverse frequent lines) reflects normal lung tissue with no consolidation and scored as zero points (Also named "A"). If less than 4 B lines (vertical lines reflecting some degree of consolidation) is observed, it refers to 1 point (named "B1"). 4 or more B lines refers to 2 points (B2), and if wide and coalesced B lines or patchy pleural line is observed that refers to 3 points (C). All evaluations will be made in supine position. In this trial, LUS will be applied in three different time points: T1: 5 minutes after orotracheal intubation T2: At the end of surgery, before extubation (under deep anesthetic state) T3: 30 minutes after extubation, in postanesthesia care unit During the surgery and the postoperative care period standart monitorization and mechanical ventilation data will be gathered. Also intraoperative and postoperative blood gas analysis will be obtained to observe oxygenation changes. This study is planned as a prospective observational study and our hypothesis is that LUS scores would be lower in acute postoperative period with robotic and laparoscopic surgeries. Therefore primary outcome is the numeric change in T3 and T1. Secondarily, LUS scores will be evaluated between robotic group and laparoscopic group patients for all time points.

NCT ID: NCT05526053 Recruiting - Weaning Failure Clinical Trials

Lung Volume Preservation During Extubation

Start date: January 15, 2023
Phase: N/A
Study type: Interventional

Introduction: At present, the best spontaneous breathing trial (SBT) during weaning from mechanical ventilation is a 30-min test with pressure support (PSV) 8 cmH2O without positive end-expiratory pressure (PEEP). There is a debate about the possible collapse of some alveolar units during such SBT and during extubation with continuous suctioning. A few experiences show extubation without suctioning as feasible and safe. Lung ultrasound is a non invasive and useful exploration tool to assess the lung aeration. Hypothesis: Techniques aimed at preserving lung volume during SBT and extubation can yield higher rates of successful extubation. The preserved lung volume of each SBT and extubation strategy can be assessed by using lung ultrasound. Primary objective: To define the rates of successful extubation in two extubation approaches aiming at different levels of lung volume preservation: standard SBT (30-min PSV 8 cmH2O without PEEP followed by extubation with continuous suctioning) versus experimental SBT (PSV8+ PEEP 5 cmH2O followed by extubation without suctioning). To define the lung aeration levels using the modified Lung Ultrasound Score (LUS) of each SBT strategy. Secondary objectives: Reintubation rate, ICU and hospital stays, and mortality in each group. To define the diaphragm and intercostal thickness and thickening fraction in different levels of lung volume preservation. Design: Prospective, multicenter, randomized study. Two opposing extubation strategies are compared in randomly assigned patients.The level of aeration is assessed using lung ultrasound.

NCT ID: NCT05345743 Recruiting - Anesthesia Clinical Trials

The Incidence of Postoperative Pulmonary Complications in Patients With a Positive and Negative AIR-Test During General Anesthesia

Start date: April 21, 2022
Phase:
Study type: Observational

The overall objective of this study is to describe the incidence of postoperative pulmonary complications in patients with a positive and negative AIR-test result. Second, the investigators wish to describe the incidence of a positive AIR-test and its association with the development of PPC. In addition, the investigators aim to describe whether mechanical ventilation strategy differs between patients with a positive and negative AIR-test.

NCT ID: NCT04830280 Recruiting - Pediatrics Clinical Trials

Effect Posterior QLB on Atelectasis

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

We aimed to investigate the effect of posterior quadratus lumborum block on postoperative atelectasis in inguinal hernia surgery in pediatric patients.

NCT ID: NCT04701541 Recruiting - Morbid Obesity Clinical Trials

Perioperative Diaphragmatic Ultrasound as Predictive Index of Atelectasis in Bariatric Surgery

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

In this study the Authors assume that peri-operative changes in DIA are predictive of postoperative atelectasis, thus providing a clinically useful tool to stratify the need for high-intensity monitoring, including admission to intensive care. Aim of this prospective observational study, in obese patients undergoing sleeve gastrectomy, is to evaluate the relationship between pre to postoperative changes in US-DIA and PaO2/FiO2.

NCT ID: NCT04235231 Recruiting - Lung Collapse Clinical Trials

The Effect of Lateral Tilt on Ventilation Distribution in Lungs Assessed by Electrical Impedance Tomography

N-LAT-EIT
Start date: June 1, 2021
Phase: N/A
Study type: Interventional

Prevention of lung inhomogeneity is an essential part of preventive strategy in neurocritical care, reducing the risks of secondary brain damage from hypoxemia, hypo/hypercapnia or pneumonia.

NCT ID: NCT04194177 Recruiting - Atelectasis Clinical Trials

Evaluation of Thoracic Impedance Tomography During Robotic Surgery

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

the evaluation of distribution of mechanical ventilation during robotic surgery

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