Prediction of Hemodynamic Reactivity During Suspension Laryngoscopy Using Analgesia/Nociception Index (ANI)

NCT01796210 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2013-06-10

No results posted yet for this study

Summary

The aim of this study is to evaluate the performance of Analgesia/Nociception Index for the prediction of hemodynamic reactivity in adult patients undergoing suspension laryngoscopy on general anesthesia.

Conditions

  • Anesthesia

Sponsors & Collaborators

  • Emmanuel Boselli

    lead OTHER

Principal Investigators

  • Emmanuel Boselli, MD, PhD · Hôpital Édouard Herriot, HCL

Eligibility

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

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2013-05-31
Completion
2013-05-31

Countries

  • France

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 NCT01796210 on ClinicalTrials.gov