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Clinical Trial Summary

This study will look at the safety, improving symptoms and decreasing the length of stay of patients admitted to the hospital with COPD.


Clinical Trial Description

The primary safety measurement for this study is the type, occurrence and severity of adverse events (anticipated and unanticipated), including serious and non-serious device-related events.

The primary outcome measure is hospital length of stay (LOS) defined as the number of days from hospital admission to the date the subject meets the medical elements of the GOLD Discharge Criteria. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01612793
Study type Observational
Source ElectroCore INC
Contact
Status Terminated
Phase
Start date October 2012
Completion date April 2013

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