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Evaluation of Analgesia Nociception Index (ANI) During Propofol/Remifentanil and Sevoflurane/Remifentanil Anesthesia

NCT01522508 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2012-06-15

No results posted yet for this study

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 propofol or sevoflurane anesthesia and changing remifentanil concentrations.

Conditions

  • General Anaesthesia

Interventions

PROCEDURE

tetanic stimulation

as test stimulus a painful tetanic stimulation is used

Sponsors & Collaborators

  • University Hospital Schleswig-Holstein

    lead OTHER

Eligibility

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

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2012-07-31
Completion
2012-10-31

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 NCT01522508 on ClinicalTrials.gov