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OpenTrials
Completed

NCT Number: NCT03778372

Methadone for Emergence Delirium in Children Undergoing Outpatient Strabismus Surgery

Strabismus surgery for children is a very common procedure, with a high incidence of emergence delirium in the recovery room. Pain is often implicated in delirium. The primary aim of this study is to determine whether a single, intraoperative dose of methadone for outpatient ambulatory pediatric strabismus surgery reduces postoperative delirium.

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • ASA I/II children undergoing outpatient strabismus surgery

Exclusion criteria

  • anything not meeting the above

Treatment and study plan

Methadone

Drug

see desc above

Primary outcomes

  1. Pediatric Anesthesia Emergence Delirium scale scores

    Time frame: measured every 10 minutes in the recovery room, until patient is discharged, up to 6 hours.

    A low total score would indicate less emergence delirium

Secondary outcomes

  1. wong-baker or numeric pain scores, depending on age

    Time frame: measured every 10 minutes in the recovery room, until patient is discharged, up to 6 hours.

    A low total score would indicate less pain

  2. discharge time

    Time frame: 24 hours

    time the patient is actually discharged from recovery room

Sponsors and collaborators

Lead sponsor

Ochsner Health System

Other

Registry information

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Dec 19, 2018
Registry last updated
Jul 19, 2022

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.

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