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Clinical Trial Summary

The aim of the present prospective randomized study was to challenge the ability of SSI to detect painful stimulation during sevoflurane - remifentanil anesthesia.


Clinical Trial Description

General anesthesia can be considered as a combination of hypnosis, antinociception and immobility. Whereas monitoring of depth of hypnosis, and muscle relaxation can be regarded as accepted, determination of the nociception is based on clinical signs like somatic or autonomic responses.

Recently, the multivariate surgical stress index (SSI)has been demonstrated to correlate with surgical stress intensity. Thus, SSI might be a useful variable to adjust analgesic drug administration in individual patients.

We want to investigate whether SSI is able to indicate nociception following standardized noxious stimulation during balanced sevoflurane - remifentanil anesthesia. ;


Study Design

Allocation: Randomized, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT00791791
Study type Interventional
Source University of Schleswig-Holstein
Contact
Status Completed
Phase N/A
Start date August 2008
Completion date November 2008

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