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Effects of Serotonin Inhibitors on Patient-controlled Analgesia Related Nausea and Vomiting

Primary Purpose

Agitation

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
agitation
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Agitation focused on measuring agitation, desflurane, children

Eligibility Criteria

2 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • tonsillectomy or adenoidectomy

Exclusion Criteria:

  • development delay,
  • CNS abnormality

Sites / Locations

    Outcomes

    Primary Outcome Measures

    agitation score
    agitation score

    Secondary Outcome Measures

    Full Information

    First Posted
    January 17, 2012
    Last Updated
    January 20, 2012
    Sponsor
    Seoul National University Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01517438
    Brief Title
    Effects of Serotonin Inhibitors on Patient-controlled Analgesia Related Nausea and Vomiting
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2012
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2011 (undefined)
    Primary Completion Date
    December 2011 (Actual)
    Study Completion Date
    December 2011 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Seoul National University Hospital

    4. Oversight

    5. Study Description

    Brief Summary
    ED50 of dexmedetomidine for prevention of emergence agitation after tonsillectomy or adenoidectomy in children

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Agitation
    Keywords
    agitation, desflurane, children

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    InvestigatorOutcomes Assessor
    Allocation
    Non-Randomized
    Enrollment
    21 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Behavioral
    Intervention Name(s)
    agitation
    Intervention Description
    agitation score after desflurane anesthesia
    Primary Outcome Measure Information:
    Title
    agitation score
    Description
    agitation score
    Time Frame
    30 minutes after postoperatuib

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    2 Years
    Maximum Age & Unit of Time
    15 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: tonsillectomy or adenoidectomy Exclusion Criteria: development delay, CNS abnormality

    12. IPD Sharing Statement

    Learn more about this trial

    Effects of Serotonin Inhibitors on Patient-controlled Analgesia Related Nausea and Vomiting

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