Status:
TERMINATED
Correlation Between NOL Index After Stimulus and Post-operative Opioid, Pain, Pre-operative Phenotype
Lead Sponsor:
Ciusss de L'Est de l'Île de Montréal
Conditions:
Pain, Postoperative
Anesthesia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This study evaluates the correlation between NoL index response to standardized stimulus under general anesthesia and the post-operative pain, assessed by opioid consumption and numerical pain scores ...
Detailed Description
The NoL index, a nociception monitor using a multiparametric approach, has shown an excellent sensitivity and specificity in detecting noxious stimuli under general anesthesia. This monitor is better ...
Eligibility Criteria
Inclusion
- Adult patient (Age 18 or older)
- ASA status I, II or III
- elective video assisted thoracoscopy under general anesthesia
Exclusion
- history of coronary artery disease
- serious cardiac arrhythmia (including atrial fibrillation),
- history of substance abuse,
- chronic use of psychotropic and/or opioid drugs,
- use of drugs that act on the autonomic nervous system (including β-blockers),
- history of psychiatric diseases,
- allergy to any drug used in the study protocol,
- refusal of the patient
- unexpected difficult airway requesting excessive, possibly painful airway manipulations
- unexpected intraoperative complications requiring strong hemodynamic support (transfusions, vasopressors, inotropes)
- conversion to thoracotomy
Key Trial Info
Start Date :
January 15 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 7 2024
Estimated Enrollment :
31 Patients enrolled
Trial Details
Trial ID
NCT03422783
Start Date
January 15 2018
End Date
March 7 2024
Last Update
July 17 2024
Active Locations (1)
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1
Hopital Maisonneuve Rosemont, CIUSSS de l'Est de l'Ile de Montreal
Montreal East, Quebec, Canada, H1T2M4