Clinical Trials Directory

Trials / Completed

CompletedNCT02942316

Pupillary Dilation Reflex (PDR) Evaluation During General Anesthesia

Pupillary Dilation Reflex (PDR) Evaluation During General Anesthesia: a Pilot Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
41 (actual)
Sponsor
University Hospital, Antwerp · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

In this study, the pupillary dilation reflex is measured as a nociceptive indicator during elective abdominal surgery under general anesthesia.

Detailed description

An infrared camera of the video pupillometer measures the pupillary dilation reflex (PDR) in response of a nociceptive stimulus. This autonomic reflex, parasympathetic mediated in sedated patients, can be generated by various pain stimuli (built in standardized protocol, surgical incision, …) The PDR is a robust reflex, even in patients under general anesthesia, and provides a potential evaluation of the autonomous circuit within the nociceptive evaluation based on pupil dilation upon A-delta and C fibers in both electrical or mechanic stimulation. This mono-centric project involving American Society of Anesthesiologists (ASA) classification I-II patients undergoing elective abdominal surgery under general anesthesia are recruited. Enrolled patients perioperative undergo PDR measurements at four different standardized times.

Conditions

Interventions

TypeNameDescription
DEVICEPupil dilation reflex measurementPupillometry (PDR) at four standardized times perioperatively * after induction, before opioid administration * after opioid administration, steady state * surgical incision * end of procedure

Timeline

Start date
2016-10-01
Primary completion
2017-04-01
Completion
2017-05-01
First posted
2016-10-24
Last updated
2018-05-21

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02942316. Inclusion in this directory is not an endorsement.