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Clinical Trial Summary

This is a randomized, prospective controlled trial in patients undergoing cardiac surgery, specifically on-pump coronary artery bypass grafting, comparing level of administered oxygen and partial pressure of arterial oxygen in the operating room and its impact on a widely-used and validated neurocognitive score, the telephonic Montreal Cognitive Assessment (t-MoCA), throughout the hospital stay and at 1 month, 3 months, and 6 postoperatively. It is hypothesized that cardiac surgical patients who undergo normoxic conditions throughout the intraoperative period will have better neurocognitive function than those with maintenance of hyperoxia.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02591589
Study type Interventional
Source Beth Israel Deaconess Medical Center
Contact
Status Active, not recruiting
Phase N/A
Start date July 2015
Completion date March 1, 2021

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