Effect of Transpulmonary MP on Prognosis of Patients With Severe ARDS Treated With VV-ECMO
Condition(s) studied
Investigational drug(s) / intervention(s)
Transpulmonary pressure: Use transpulmonary pressure to guide ventilator setting in ECMO for severe ARDS patients.
Study summary
Venovenous extracorporeal membrane oxygenation (VV-ECMO) is a salvage treatment for severe acute respiratory distress syndrome (ARDS). With the large-scale implementation of VV-ECMO in critical care medicine departments in China, significant progress has been made in treating severe ARDS. However, the patient mortality rate remains high. The pathophysiological essence of ARDS is an imbalance between the body's oxygen supply and demand, causing tissue and cell hypoxia, organ dysfunction, and even death. The VV-ECMO treatment process still requires mechanical ventilation assistance. However, inappropriate mechanical ventilation settings can lead to ventilator-related lung injury (VILI). In recent years, mechanical power has gradually attracted everyone's attention and is considered the cause of VILI. The transpulmonary mechanical power is more accurate to the energy directly performed to the lung tissue. Transpulmonary mechanical energy has a specific value in judging the prognosis of mechanically ventilated patients, but its clinical significance in treating patients with VV-ECMO is unclear. This study aimed to explore the value of transpulmonary mechanical power in predicting the prognosis of patients with severe ARDS patients treated with VV-ECMO.
Eligibility
Primary outcome measure(s)
- Patients successfully weaned from VV-ECMO — After patients enrolled 60 days
Weaning VV-ECMO more than 48 hours with stable oxygenation and no need to re-establish ECMO
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Beijing Chao-Yang Hospital | Beijing | Beijing Municipality | Recruiting |
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Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06062212 on ClinicalTrials.gov ↗ ← All trials in China