Clinical Trials Directory

Trials / Completed

CompletedNCT00791791

Evaluation of Surgical Stress Index (SSI) During Sevoflurane/Remifentanil Anesthesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
24 (actual)
Sponsor
University Hospital Schleswig-Holstein · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREstandardized pain stimulusa tetanic stimulus (30s, 50 Hz, 60mA) applied as standardized pain stimulus

Timeline

Start date
2008-08-01
Primary completion
2008-11-01
Completion
2008-11-01
First posted
2008-11-17
Last updated
2012-06-15

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00791791. Inclusion in this directory is not an endorsement.