Prediction of Hemodynamic Reactivity During General Anesthesia Using Analgesia/Nociception Index (ANI)
NCT ID: NCT01839513
Last Updated: 2013-11-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
100 participants
OBSERVATIONAL
2013-05-31
2013-11-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Ear-nose-throat or lower limb surgery
* General anesthesia using desflurane and remifentanil
Exclusion Criteria
* Arrythmia
* Preoperative use of B-blockers
* Administration of anticholinergic drugs or neuromuscular blockade reversal in the 20 previous minutes
* Psychiatric diseases
* Autonomic nervous system disorders (epilepsy)
18 Years
75 Years
ALL
No
Sponsors
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Hôpital Edouard Herriot
OTHER
Responsible Party
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Emmanuel Boselli
MD, PhD
Principal Investigators
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Emmanuel Boselli, MD, PhD
Role: STUDY_DIRECTOR
Hôpital Edourd Herriot
Bernard Allaouchiche, MD, PhD
Role: STUDY_CHAIR
Hôpital Edouard Herriot
Locations
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Hôpital Édouard Herriot, HCL
Lyon, Rhône, France
Countries
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References
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Boselli E, Daniela-Ionescu M, Begou G, Bouvet L, Dabouz R, Magnin C, Allaouchiche B. Prospective observational study of the non-invasive assessment of immediate postoperative pain using the analgesia/nociception index (ANI). Br J Anaesth. 2013 Sep;111(3):453-9. doi: 10.1093/bja/aet110. Epub 2013 Apr 16.
Other Identifiers
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CPP 2013-021B
Identifier Type: -
Identifier Source: org_study_id