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Continuous Regional Analysis Device for Neonate Lung — CRADL  

Acute Respiratory Distress Syndrome Clinical Trial

Official title:
Continuous Regional Analysis Device for Neonate Lung

Clinical Trial Summary

The purpose of the study is to assess whether Electrical Impedance Tomography (EIT) has the potential to optimize the ventilator therapy, validate the effectiveness, efficacy and safety of nursing and medical interventions (endotracheal suctioning, posture changes, surfactant therapy, recruitment manoeuvres, etc.) and for early recognition of complications like pneumothorax and endotracheal tube misplacement. The study design is purely observational.

Clinical Trial Description

EIT data will be recorded during 72 hours of routine clinical treatment. To prevent any decisions based on EIT information, the clinicians will be blinded to the EIT findings during the study period. Data on clinical interventions and clinical findings will be recorded using a specially adapted graphical user interface on the EIT device in combination with a paper-based case report form (CRF). EIT data analysis will be performed off-line. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02962505
Study type Observational
Source University of Schleswig-Holstein
Contact
Status Completed
Phase
Start date November 2016
Completion date March 3, 2019
View Details
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