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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | standardized pain stimulus | a 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.