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

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

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Key information

Conditions

Pain Anesthesia Neurologic Manifestations Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

2 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Departement d'anesthesie Hopital Armand Trousseau

Paris, 75012, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Elective surgery under general anesthesia
Written informed consent

Exclusion criteria

Chronic pain
Preoperative analgesic drug
Neurologic disease
Ophtalmic disease

Treatment and study plan

alfentanil

Drug

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

Sevoflurane or Propofol

Drug

Primary outcomes

Change between Pupillary Pain Index before and after alfentanil bolus

Time frame: Five minutes before incision and just before incision. Each measure = 20 seconds

pupillometry

Sponsors and collaborators

Lead sponsor

Pr Isabelle CONSTANT

Other

Registry information

Important dates

Study start: 2016
Primary completion: 2016
Study completion: 2016
First posted: Jan 5, 2016
Registry last updated: May 3, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed