NCT04000126View on ClinicalTrials.gov

Pupillometry - Future of Objective Pain Reaction Measurement While Unconscious

NACompletedINTERVENTIONAL
Enrollment

90

Participants

Timeline

Start Date

February 25, 2019

Primary Completion Date

November 30, 2019

Study Completion Date

December 31, 2019

Conditions
Pain
Interventions
DEVICE

Pupil reflex dilation measurement (PRD)

Pupillary Reflex Dilation (PRD) measured for 60 s during orotracheal intubation using a video pupillometer

DEVICE

PPI (Pupillary Pain Index)

Pupillary Reflex Dilation (PRD) measured using a video pupillometer 5 min after orotracheal intubation

DRUG

lidocaine

1.5 mg/kg lidocaine/ 100ml 0,9% NaCl iv 10min before intubation

DRUG

Placebo

100ml 0,9% NaCl iv 10min before intubation

DEVICE

Bispectral Index (BIS)

Bispectral Index will be monitored to assess the depth of anaesthesia

DEVICE

HR

HR in beats/min will be measured by the electrocardiogram monitor

DEVICE

BP

BP will be measured automatically by an occluding upper arm cuff

Trial Locations (1)

11-041

Anesthesiology and Intensive Care Clinical Ward, Clinical University Hospital, Olsztyn

All Listed Sponsors
lead

University of Warmia and Mazury

OTHER

NCT04000126 - Pupillometry - Future of Objective Pain Reaction Measurement While Unconscious | Biotech Hunter | Biotech Hunter