Clinical Trials Logo

Clinical Trial Summary

The extubation phase is a risky period of anesthesia management. During this step, serious complications can arise: hypoxemia, laryngospasm, pharyngeal obstruction, pneumonia… In spite of these complications, extubation and its impact on respiratory function, particularly on the Functional Residual Capacity (FRC), remains poorly studied because of the difficulty to make bedside measurements. The PulmoVista 500 is a clinical routine which provide effective non-invasive bedside measurements. It would be interesting to evaluate the impact of extubation on respiratory function, and more specifically FRC changes during and after extubation. This study will allow a better physiopathological knowledge and a quality improvement patient extubation management.


Clinical Trial Description

The aim of this study is to evaluate the variation of functional residual capacity and its distribution before and after extubation. Patients with scheduled surgery and receiving general anesthesia with orotracheal intubation are included and the measurements will be performed in the post-interventional monitoring room (PICU). EELI data will be collected before extubation and then at T0, then T5, T10, T15 and T20 minutes. No subsequent follow-up is required. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05077605
Study type Interventional
Source Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Contact
Status Completed
Phase N/A
Start date November 5, 2021
Completion date June 30, 2022

See also
  Status Clinical Trial Phase
Completed NCT00779090 - Functional Residual Capacity (FRC) Guided Alveolar Recruitment Strategy Phase 4
Completed NCT00669383 - Rescue Antenatal Steroids and Pulmonary Function Tests in Preterm Infants N/A
Completed NCT01962818 - High Frequency Oscillatory Ventilation Combined With Intermittent Sigh Breaths: Effects on Lung Volume Monitored by Electric Tomography Impedance. N/A
Not yet recruiting NCT03511651 - The Effect of Positive End-Expiratory Pressure on Functional Residual Capacity During Mechanical Ventilation N/A