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Effect of a Bolus of 10 µg/kg of Alfentanil on the Pupillary Pain Index

NCT02646592 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2017-05-03

No results posted yet for this study

Summary

This study aims to assess the Pupillary Pain Index before and after a bolus of alfentanil in children under general anesthesia, before skin incision.

Conditions

Interventions

DRUG

Alfentanil

Bolus of alfentanil 10 µg/kg 5 minutes before skin incision

DRUG

sevoflurane or propofol

Sponsors & Collaborators

  • Pr Isabelle CONSTANT

    lead OTHER

Principal Investigators

  • Isabelle Constant, PHD · University Hospital Armand Trousseau

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
2 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2016-10-31
Completion
2016-12-31

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02646592 on ClinicalTrials.gov