Status:
COMPLETED
Prediction of Hemodynamic Response to Intubation by ANI Variation During Standardized Stimulation
Lead Sponsor:
University Hospital, Lille
Conditions:
Tracheal Intubation Morbidity
Pain
Eligibility:
All Genders
18-99 years
Phase:
NA
Brief Summary
The objective : to investigate a correlation between ANI following a standardized nociceptive stimulus and hemodynamic or somatic reactions during orotracheal intubation. Piloted study. ANI and hemod...
Detailed Description
Background: The Analgesia Nociception Index reflects the balance between analgesia and nociception and allows early detection of a defect in analgesia. Orotracheal intubation is responsible for a some...
Eligibility Criteria
Inclusion
- Any patient requiring general anaesthesia with tracheal intubation by direct laryngoscopy
- Intubation Difficulty Assessment Score \< 7
- BMI between 17 and 30 Kg/m2
- Socially insured patient
- Patient 18 years of age or older
- Patient with signed consent
- Patient with a sinus heart rhythm
Exclusion
- Patient refusing to participate in the study
- Pregnant woman
- Patient with a pace maker (any mode)
- Patient treated with Beta Blocker
- Known Dysautonomia
- Diabetes
- Spontaneous ventilation anaesthesia
- Allergy to any of the required medications
Key Trial Info
Start Date :
February 2 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2014
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT04354311
Start Date
February 2 2014
End Date
December 1 2014
Last Update
December 22 2025
Active Locations (1)
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1
Hopital Roger Salengro, CHU Lille
Lille, France, 59037