NCT03140241View on ClinicalTrials.gov

Pain Assessment by Pupil Dilation Reflex (PDR) and Pupillary Pain Index (PPI) in Response to Noxious Stimulation in Anesthetized Adults

NACompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

May 7, 2017

Primary Completion Date

June 29, 2017

Study Completion Date

July 20, 2017

Conditions
Nociceptive PainMonitoring, Intraoperative
Interventions
PROCEDURE

PDR measurement

"PDR measurement at two standardized times perioperatively:~1. : anesthetized subject by propofol sedation until sedation depth monitor NeuroSense® (NeuroWave Systems Inc, Cleveland, OH) between 40-50~2. : administration of remifentanil via effect site target concentration (Minto-model) at 5 ng/ml, in the absence of adjustments in sedation depth"

Trial Locations (1)

2650

University hospital Antwerp, Edegem

All Listed Sponsors
lead

University Hospital, Antwerp

OTHER

NCT03140241 - Pain Assessment by Pupil Dilation Reflex (PDR) and Pupillary Pain Index (PPI) in Response to Noxious Stimulation in Anesthetized Adults | Biotech Hunter | Biotech Hunter