Status:
COMPLETED
Pupillary Response to Incremental Tetanic Stimulations Under Propofol-remifentanil TCI
Lead Sponsor:
Pr Isabelle CONSTANT
Conditions:
Pain
Eligibility:
FEMALE
18-65 years
Phase:
NA
Brief Summary
In patients under standardized steady-state general anesthesia, 6 tetanic stimulations of incremental intensities were applied to the patients. Pupillary dilation in response to these stimulations was...
Detailed Description
The aim of the study was to investigate a possible correlation between the intensity of a nociceptive stimulus and the magnitude of pupillary reflex dilation in patients anesthetized with propofol and...
Eligibility Criteria
Inclusion
- Scheduled gynecological surgery requiring general anesthesia and orotracheal intubation
- written informed consent
Exclusion
- ophthalmic disease
- neurologic disease
- preoperative chronic pain or pain medication
- medication interfering with autonomous nervous system (beta blockers, alpha agonists, metoclopramide, droperidol, atropine, catecholamines)
Key Trial Info
Start Date :
January 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2013
Estimated Enrollment :
18 Patients enrolled
Trial Details
Trial ID
NCT04465773
Start Date
January 1 2012
End Date
July 1 2013
Last Update
July 10 2020
Active Locations (1)
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1
Departement d'anesthesie Hopital Armand Trousseau
Paris, France, 75012