NCT04786275View on ClinicalTrials.gov

Evaluation of the Nociception Guided by NoL Index and PK of Fentanyl in Pediatric Patients Under General Anesthesia

CompletedOBSERVATIONAL

Enrollment

Participants

Timeline

Start Date

December 1, 2020

Primary Completion Date

December 31, 2022

Study Completion Date

March 31, 2023

Conditions

PainAnesthesiaPediatric ALL

Interventions

DRUG

Fentanyl

Standard dose of 2 ug/kg after tetanic stimulation.

OTHER

Tetanic stimulation

Standard tetanic stimulation will be used as the stimulus to evaluate response of the intraoperative pain index (NoL) at a standard fentanyl dose.

Trial Locations (1)

Unknown

Pontificia Universidad Catolica de Chile, Santiago

All Listed Sponsors

lead

Pontificia Universidad Catolica de Chile

OTHER

NCT04786275 - Evaluation of the Nociception Guided by NoL Index and PK of Fentanyl in Pediatric Patients Under General Anesthesia | Biotech Hunter | Biotech Hunter