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Clinical Trial Summary

The AirSeal® System will allow for lower carbon dioxide (CO2) absorption rates than the standard Endopath System.


Clinical Trial Description

The primary observation to be made is the level of carbon dioxide in the arterial blood, specifically when the patient is insufflated and deflated during the surgery. As a result of the consistent pressure that the AirSeal® system maintains, carbon dioxide will be absorbed in lower levels when compared to the standard of care systems in which fluctuations in intra-peritoneum pressure are seen. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02114164
Study type Interventional
Source OhioHealth
Contact
Status Completed
Phase N/A
Start date August 2016
Completion date July 15, 2019

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