MetaNeb® Chest X-ray Study

Status Completed

Clinical Trial Summary

To study objective is to evaluate the impact of use of The MetaNeb® System in clearance of atelectasis, as demonstrated by improvement in chest x-rays. This is a a non-randomized open label study, with all subjects receiving treatment with The MetaNeb® System. Subjects who qualify for enrollment in the study will receive therapy with The MetaNeb® System following the labeled instructions for the device. Details of the treatment including duration and frequency will be defined in treatment procedures.

Clinical Trial Description

Study Population: Post-surgical (thoracic, cardiac or abdominal surgery) non-mechanically ventilated patients with significant atelectasis as documented by chest x-ray results. Duration of treatment: Duration of treatment with The MetaNeb® System will be a minimum of 48 hours, or until the subject is discharged from the hospital (if discharge is earlier). Enrolled subjects will remain in the study through Day 4 or until the subject is discharged from the hospital, whichever occurs sooner. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02871258
Study type	Interventional
Source	Baxter Healthcare Corporation
Contact
Status	Completed
Phase	N/A
Start date	September 2016
Completion date	August 17, 2017

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