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Clinical Trial Summary

Patients were randomized into 2 groups according to the anesthetic, propofol or sevoflurane. Induction and maintenance were standardized, and after the end of surgery, two steady-state recordings were performed at BIS 25 and BIS 55. Bispectral Index and ECG were continuously recorded and cardiac autonomic nervous activity was investigated using spectral analysis of RR Interval variability


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03098875
Study type Interventional
Source Hôpital Armand Trousseau
Contact
Status Completed
Phase N/A
Start date January 2009
Completion date September 2010

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