A Comparison of Different Ventilation Strategies in Children Using the Proseal™ Laryngeal Mask Airway

This study has been completed.
Sponsor:
Information provided by:
Wake Forest University
ClinicalTrials.gov Identifier:
NCT00966433
First received: August 25, 2009
Last updated: August 4, 2011
Last verified: July 2010

August 25, 2009
August 4, 2011
August 2009
October 2009   (final data collection date for primary outcome measure)
Differences in end-tidal carbon dioxide and tidal volume compared between the spontaneous ventilation and pressure support ventilation groups. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00966433 on ClinicalTrials.gov Archive Site
  • Differences in respiratory rates between spontaneous ventilation and pressure support ventilation groups. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Mean values of respiratory rate compared between the spontaneous ventilation and pressure control ventilation groups. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Mean values of respiratory rate compared between pressure support ventilation and pressure control ventilation groups. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
A Comparison of Different Ventilation Strategies in Children Using the Proseal™ Laryngeal Mask Airway
A Comparison of Different Ventilation Strategies in Children Using the Proseal™ Laryngeal Mask Airway

The purpose of this research study is to compare difference between breathing by oneself or with the partial help from an anesthesia machine in children under general anesthesia.

The laryngeal mask airway (LMA) is a breathing device that sits above the vocal cords and allows the patient to breathe in and out adequately under general anesthesia (GA). The ProSeal™ LMA (PLMA™) is a specialized type of LMA with a design that permits the delivery of higher pressures to help the patient breathe in and out (ventilate) and also contains a channel to suction the stomach.

Children under GA may breathe through a PLMA in different ways. Spontaneous ventilation consists of the children breathing on their own through a PLMA™. Pressure support ventilation allows the patient to breathe on their own with additional help from the anesthesia machine. Pressure control ventilation allows the patient to breathe with the help of an anesthesia machine.

A child undergoing surgery requires a deep level of general anesthesia which negatively affects their ability to ventilate. Thus, children may not breathe in oxygen and carbon dioxide out adequately at this level of anesthesia and it may be beneficial to provide some level of support to enhance carbon dioxide exchange and to avoid hypoventilation.

This study will attempt to determine whether pressure support ventilation improves ventilation in children undergoing outpatient surgery.

Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Ventilation
  • Procedure: Spontaneous ventilation
    The patient will breathe spontaneously (on their own)while under general anesthesia throughout the duration of the surgery.
  • Procedure: Pressure support Ventilation
    The patient will breathe on their own and with a little assistance from the anesthesia machine while under general anesthesia throughout the duration of the surgery.
  • Procedure: Pressure control ventilation
    The patient's ventilation will be completely supported by the anesthesia machine while under general anesthesia throughout the duration of the surgery.
  • Experimental: Spontaneous ventilation
    Intervention: Procedure: Spontaneous ventilation
  • Experimental: Pressure support ventilation
    Intervention: Procedure: Pressure support Ventilation
  • Active Comparator: Pressure control ventilation
    Intervention: Procedure: Pressure control ventilation

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
33
October 2009
October 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • ASA physical classification 1,2 (Healthy or relatively healthy children)
  • Subjects scheduled for outpatient surgical procedures.
  • Surgical procedure anticipated to be < 90 minutes
  • Subject weight of ≤ 20 kg (44 lbs)
  • Subject age of 12 months to 5 years (inclusive)

Exclusion Criteria:

  • Inpatient
  • ASA physical classification of 3, 4 or E (sick children)
  • Risk of aspiration
  • Subjects with malignant hyperthermia or family history of malignant hyperthermia
  • Subjects with tracheostomies
Both
12 Months to 5 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00966433
PLMA study WFU
No
Thomas Wesley Templeton, M.D., Wake Forest University Health Sciences
Wake Forest University
Not Provided
Principal Investigator: Thomas W Templeton, M.D. Wake Forest University
Wake Forest University
July 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP