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Non-invasive Assessment of Immediate Postoperative Analgesia Using Analgesia/Nociception Index (ANI)

NCT01633320 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2012-12-18

Study results available
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Summary

The aim of this study is to evaluate the clinical performance on Analgesia/Nociception Index (ANI) in the assessment of immediate postoperative analgesia in PACU in adult patients undergoing general anesthesia.

Conditions

  • Postoperative Pain

Sponsors & Collaborators

  • Hôpital Edouard Herriot

    lead OTHER

Principal Investigators

  • Lionel Bouvet, MD · Édouard Herriot hospital, HCL

  • Gérard Bégou, MD · Édouard Herriot hospital, HCL

  • Rabia Dabouz, MD · Édouard Herriot hospital, HCL

  • Christophe Magnin, MD · Édouard Herriot hospital, HCL

  • Bernard Allaouchiche, MD, PhD · Édouard Herriot hospital, HCL

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

  • Mirela-Daniela Ionescu, MD · Édouard Herriot hospital, HCL

Eligibility

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

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2012-07-31
Completion
2012-07-31

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 NCT01633320 on ClinicalTrials.gov