Effect of Duration of Exposure of Anesthesia With Sevoflurane on Emergence Delirium

Sponsor
State University of New York - Upstate Medical University (Other)
Overall Status
Unknown status
CT.gov ID
NCT02509221
Collaborator
(none)
114
1

Study Details

Study Description

Brief Summary

Emergence delirium which is a phenomenon seen commonly in preschool kids anesthetized with Sevoflurane. Restless recovery from anesthesia may not only cause injury to the child or to the surgical site, but may also lead to the accidental removal of surgical dressings, IV catheters, and drains. is one of the The purpose of the study is to find whether duration of exposure to Sevoflurane has any effect on the incidence of Emergence Delirium.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    114 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Study Start Date :
    Jul 1, 2015
    Anticipated Primary Completion Date :
    May 1, 2016

    Arms and Interventions

    Arm Intervention/Treatment
    Less than 30 minutes

    30-60 minutes

    More than 60 minutes

    Outcome Measures

    Primary Outcome Measures

    1. Incidence of emergence delirium [30 mintes after anesthesia]

      using the PAED scale

    2. Severity of emergence delirium [30 minutes after anesthesia]

      using the PAED scale

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Year to 6 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • age between 1-6 years of age

    • receiving general anesthesia for non-surgical procedure

    Exclusion Criteria:
    • history of emergence delirium

    • severe CNS disease

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital Syracuse New York United States 13210

    Sponsors and Collaborators

    • State University of New York - Upstate Medical University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Joseph Resti, MD, State University of New York - Upstate Medical University
    ClinicalTrials.gov Identifier:
    NCT02509221
    Other Study ID Numbers:
    • 714457
    First Posted:
    Jul 27, 2015
    Last Update Posted:
    Jul 27, 2015
    Last Verified:
    Jul 1, 2015
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 27, 2015