Status:
UNKNOWN
Evaluation of Analgesia Nociception Index (ANI) During Propofol/Remifentanil and Sevoflurane/Remifentanil Anesthesia
Lead Sponsor:
University Hospital Schleswig-Holstein
Conditions:
General Anaesthesia
Eligibility:
All Genders
18-65 years
Brief Summary
The aim of this prospective randomized study was to evaluate the ability of the new Analgesia Nociception Index ANI, derived by heart rate variability, to detect painful stimulation during either prop...
Detailed Description
Monitoring Antinociception during general anesthesia is still a big challenge in the field and has not become clinical routine yet. Recently, for the Surgical Pleth Index SPI a benefit for the patient...
Eligibility Criteria
Inclusion
- age between 18- 65 years,
- ASA physical status I or II,
- elective surgery in general anesthesia planned,
- written informed consent
Exclusion
- pregnancy,
- history of cardiac arrhythmia,
- presents of any neuromuscular or neurologic disease,
- use of CNS-active medication or abuse of alcohol/illicit drugs -
Key Trial Info
Start Date :
June 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
October 1 2012
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT01522508
Start Date
June 1 2011
End Date
October 1 2012
Last Update
June 15 2012
Active Locations (1)
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1
University Hospital Kiel, Dept. of Anesthesiology and Intensive Care Med.
Kiel, Germany, 24105