Temperature Changes During Induction of General Anesthesia in Pediatric Patients

Sponsor
University of Oklahoma (Other)
Overall Status
Completed
CT.gov ID
NCT00710320
Collaborator
(none)
44
1
8
5.5

Study Details

Study Description

Brief Summary

We aim that uncovering patients during induction of general anesthesia does not decrease core body temperature in pediatric patients.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Covered and uncovered anesthesia induction

Detailed Description

Some anesthesiologists cover the pediatric patient with a blanket during the induction of general anesthesia, while others do not. Complaints have been raised by pediatric surgeons that if a pediatric patient is not covered during induction of general anesthesia, the child's core body temperature will be lower than normal following surgery and in the recovery room.

Children are at risk of significant heat loss in the operating room due to multiple factors, such as, exposure to cold temperatures, decrease in metabolism following induction of general anesthesia, increased surface-area-to-volume ratio, and through considerable respiratory heat loss.1

A decrease in temperature of 0.5ºC to 1.5ºC can occur during induction of general anesthesia in pediatric patients2. The use of heating blankets and warmers may increase temperature or result in a constant temperature on pediatric patients intra-operatively3. We want to investigate the differences in temperature between the two approaches, covering and not covering pediatric patients, during induction of general anesthesia of a urologic procedure with a caudal block and the difference in temperature post-operatively. We hypothesize that the core temperatures of:

  1. the covered and warmed group during induction of general anesthesia will be greater by 0.5ºC than the uncovered group during induction of general anesthesia.

  2. both groups, covered and uncovered, will be equal during surgery and post-operatively. In other words, due to the active warming procedures during surgery and post-operatively in the PICU, core temperatures of the uncovered group will catch up to the covered group.

Study Design

Study Type:
Observational
Actual Enrollment :
44 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Temperature Changes During Induction of General Anesthesia in Pediatric Patients
Study Start Date :
Jul 1, 2008
Actual Primary Completion Date :
Mar 1, 2009
Actual Study Completion Date :
Mar 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Cover and Uncover

Procedure/Surgery

Procedure: Covered and uncovered anesthesia induction
We hypothesize that the core temperatures of: the covered group during induction of general anesthesia will be greater by 0.5ºC than the uncovered group during induction of general anesthesia. both groups, covered and uncovered, will be equal during surgery and post-operatively. In other words, due to the active warming procedures during surgery and post-operatively in the PICU, core temperatures of the uncovered group will catch up to the covered group.
Other Names:
  • Temperature
  • Pediatric
  • Urology
  • Anesthesia
  • Outcome Measures

    Primary Outcome Measures

    1. Covered group during induction of general anesthesia will be greater by 0.5ºC than the uncovered group during induction of general anesthesia. [1.5 years]

    Secondary Outcome Measures

    1. Covered and uncovered, will be equal during surgery and post-operatively. In other words, due to the active warming procedures during surgery and post-operatively in the PICU, core temperatures of the uncovered group will catch up to the covered group. [1.5 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Months to 3 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • The ages of the subjects ranging from 6 months to 3 years undergoing surgery for circumcision or hernia repair with caudal block.
    Exclusion Criteria:
    • ASA physical status classification greater than 2, unsigned or unattainable written informed consent form, induction of general anesthesia time of greater than 45 minutes, fever, or temperature regulation inability.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The University of Oklahoma Health Sciences Center Deparment of Anesthesiology Oklahoma City Oklahoma United States 73104

    Sponsors and Collaborators

    • University of Oklahoma

    Investigators

    • Principal Investigator: Mohanad Shukry, MD, The University of Oklahoma Health Sciences Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00710320
    Other Study ID Numbers:
    • IRB No 14004
    First Posted:
    Jul 4, 2008
    Last Update Posted:
    Feb 4, 2010
    Last Verified:
    Feb 1, 2010
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 4, 2010