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

NCT00791791 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2012-06-15

No results posted yet for this study

Summary

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

Conditions

  • Analgesia

Interventions

PROCEDURE

standardized pain stimulus

a tetanic stimulus (30s, 50 Hz, 60mA) applied as standardized pain stimulus

Sponsors & Collaborators

  • University Hospital Schleswig-Holstein

    lead OTHER

Principal Investigators

  • Matthias Gruenewald, MD · Department of Anaesthesiology and Intensive Care Medicine, University Hospital Schleswig-Holstein, Campus Kiel

  • Berthold Bein, MD, DEAA · Department of Anaesthesiology and Intensive Care Medicine, University Hospital Schleswig-Holstein, Campus Kiel

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2008-11-30
Completion
2008-11-30

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00791791 on ClinicalTrials.gov