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Lung Injury clinical trials

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NCT ID: NCT03061617 Completed - Thoracic Surgery Clinical Trials

Comparison of Different Ventilation Mode During One-lung Ventilation

Start date: July 2016
Phase: N/A
Study type: Interventional

It is controversial as to which ventilation mode is better in one-lung ventilation(OLV), volume controlled ventilation(VCV) or pressure controlled ventilation(PCV). This study was designed to figure out if there was any difference between these two modes on oxygenation and postoperative complications under the condition of protective ventilation(PV).

NCT ID: NCT03056885 Completed - Clinical trials for Inflammatory Response

Inflammatory Local Response During OLV: Protective vs Conventional Ventilation Strategy

Start date: November 2, 2015
Phase: N/A
Study type: Interventional

This study evaluates the local cytokine inflammatory response during one lung ventilation in patients undergoing pulmonary lobectomy or wedge resection. We compare two different ventilation strategies: a conventional strategy with a protective strategy.

NCT ID: NCT03041428 Completed - Clinical trials for Ventilator-Induced Lung Injury

Ultra Protective Ventilation During Venoarterial Extracorporeal Membrane Oxygenation (UPV-ECMO)

UPV-ECMO
Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Mechanical ventilation, in spite of being a life-saving technique, can also induce lung injury (VILI) mediated by an inflammatory response, thus having a profound impact in the course of critically ill patients. Ventilatory strategies aimed to minimize this VILI have reduced mortality rates. Patients suffering cardiogenic pulmonary edema may need venoarterial extracorporeal oxygenation, at the same time they are being mechanically ventilated. The objective of this study is to analyze changes induced by the use of utraprotective ventilatory strategies in the inflammatory lung response of these patients and their impact on outcomes.

NCT ID: NCT03023670 Completed - Lung Injury, Acute Clinical Trials

Lung Protection and Pediatric Cardiac Surgery

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

The lung is at risk for ischemic insults during total cardiopulmonary bypass because lung perfusion is maintained solely by the bronchial arterial system

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: NCT03016182 Recruiting - Lung Injury Clinical Trials

Remote Ischemic Preconditioning on Pulmonary Injury in Cardic Surgery

Start date: February 7, 2017
Phase: N/A
Study type: Interventional

During cardiac surgery with cardiopulmonary bypass , pulmonary dysfunction remains to be a problem complicating the postoperative course of the patients.Remote ischemic preconditioning(RIPC) with transient upper limb ischemia/reperfusion is a novel, simple, cost-free,non-pharmacological and non-invasive strategy.Recent several trials suggested that RIPC could provide pulmonary protection by reducing serum biomarkers,however,whether the RIPC can improve the clinical outcomes in patients undergoing on-pump cardiac surgery,is still uncertain. The study hypothesis is: remote ischemic preconditioning will provide lung-protective effect and improve clinical outcomes in patients undergoing cardic surgery.

NCT ID: NCT02978885 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Imaging of Peri-operative (periOP) Lung Injury

Start date: June 11, 2018
Phase: Phase 2
Study type: Interventional

The aim of study is to determine if 99mTc Annexin V-128 (AxV- 128/Tc) single photon emission computed tomography (SPECT)-computed tomography (CT) can detect perioperative lung injury. The investigators will study patients undergoing major surgery, specifically Whipple procedures (pancreatico-duodenectomies) and compare AxV-128/Tc SPECT-CT scans before and after surgery in Chronic Obstructive Pulmonary Disease (COPD) and non-COPD patients.

NCT ID: NCT02977676 Completed - Clinical trials for Ventilator-Associated Lung Injury

Ventilator-Associated Events: Prevalence, Outcome and Preventability

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

The aim of this study is to determine the prevalence of ventilator-associated events (VAE). To analyze the patients profile, morbidity and mortality compared to patients who did not develope VAE. The preventability of VAE will be assessed by comparing the percentage of adherence to the bundle of preventive measures among patients who developed and did not develope VAE.

NCT ID: NCT02948530 Recruiting - Acute Lung Injury Clinical Trials

Measurement of Lung Elastance and Transpulmonary Pressure Using Two Different Methods (Lungbarometry)

Start date: October 2016
Phase:
Study type: Observational

Classically lung elastance and transpulmonary pressure are measured from the difference in tidal variations of airway pressure subtracted by tidal variations i esophagus pressure divided by the tidal volume. This requires the presence of a esophageal balloon catheter which is cumbersome and costly. In this study values obtained as described above are compared to values obtained with a new method in which a stepwise increase in positive endexpiratory pressure (PEEP) is performed with a size of the lung volume increase which corresponds to the tidal volume which the patient is ventilated with. The measurements are performed in sedated and mechanically ventilated patients in the intensive care unit.

NCT ID: NCT02918877 Completed - Clinical trials for Postoperative Pulmonary Complications

Anesthetics to Prevent Lung Injury in Cardiac Surgery

APLICS
Start date: June 9, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate whether the use of inhaled anesthetics, compared to intravenous anesthetics, can affect the amount of lung inflammation and postoperative respiratory complications seen after cardiac surgery.