Clinical Trials Directory

Trials / Unknown

UnknownNCT05767125

Effect of APRV and LTV on Lung Ventilation and Perfusion in Patients With Moderate-to-severe ARDS

Effect of APRV and LTV on Lung Ventilation and Perfusion in Patients With Moderate-to-severe ARDS: a Single-center, Pilot Randomized Controlled Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

Low tidal volume ventilation (LTV) has been proposed and widely used in patients with acute respiratory distress syndrome (ARDS) to prevent ventilator-induced lung injury (VILI) and mitigate its effects. The LTV strategy is intended to protect the "baby lung" from overdistension while simultaneously allowing acutely injured tissue to continually collapse. Airway pressure release ventilation (APRV) is a highly effective strategy improving lung recruitment and oxygenation in clinical studies, but its effects on lung injury and mortality is debatable. Animal studies revealed that APRV could normalize post-injury heterogeneity and reduce the risk of VILI. Our objective was to investigate the impact of APRV and LTV on regional ventilation and perfusion distribution in ARDS patients by electrical impedance tomography (EIT).

Conditions

Interventions

TypeNameDescription
DEVICEAPRVPatients with moderate-to-severe ARDS were supported with APRV.
DEVICELTVPatients with moderate-to-severe ARDS were supported with LTV.

Timeline

Start date
2023-01-01
Primary completion
2024-12-31
Completion
2024-12-31
First posted
2023-03-14
Last updated
2023-03-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05767125. Inclusion in this directory is not an endorsement.