Clinical Trials Directory

Trials / Completed

CompletedNCT03237806

Effects of Sedation on Transpulmonary Pressure and Lung Homogenous

Effects of Sedation on Transpulmonary Pressure and Lung Homogenous of ARDS Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Southeast University, China · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The acute respiratory distress syndrome (ARDS) is characterized by severe respiratory failure. Open Lung and Lung Protective Strategy have been proved to improve mortality of ARDS patients. Preserving spontaneous breathing (SB) is good for inflating the lung lobe near diaphram during mechanical ventilation, however, strong respiratory drive could generate more transpulmonary pressure in ARDS patients, which increase the stress and strain in injured lung. Nonetheless, it's not clear if sedative has any effects on transpulmonary pressure of ARDS patients.The purpose of this study is to investigate the effects of sedation on transpulmonary pressure of ARDS patients.

Detailed description

Further study details as provided by Nanjing Zhong-da Hospital, School of Medicine, Southeast University

Conditions

Interventions

TypeNameDescription
DRUGDeep sedatedMidazolam intravenous continusly infusion, Deep sedated (Ramsay 5)
DRUGLight sedatedMidazolam intravenous continusly infusion, Light sedated (Ramsay 3)

Timeline

Start date
2015-05-31
Primary completion
2018-01-18
Completion
2018-03-18
First posted
2017-08-03
Last updated
2018-03-20

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03237806. Inclusion in this directory is not an endorsement.