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Completed

NCT Number: NCT01394172

A Novel Method of Non-invasive Ventilation in Children

The purpose of this study is to quantify the tidal volume generated by the pressure release immediately following the application of pressure to the chest.

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Key information

Age range

1 day–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Stollery Children's Hospital

Edmonton, Alberta, T6G 2B7, Canada

About this study

Airway management in the pediatric population differs from the adult population because of differences in their respiratory physiology and anatomy. For example the oxygen consumption is about three times higher in children as compared to adults; therefore, if there is a problem ventilating a child there is a higher impact on oxygen delivery and oxygen reserve. Current guidelines recommend that in respiratory emergencies where one "cannot ventilate and cannot intubate" that a cricothyroidectomy (insertion of a needle through the cricothyroid membrane in the neck) be performed. This procedure is very invasive and difficult to perform, especially in a small child. Since timing and simplicity are essential to successful airway management it is hypothesized that the investigators could utilize the physiological principles behind breathing to ventilate these children using the release of applied pressure to their chest. During, inspiration, the vertical and transverse dimensions of the thorax are increased, generating a negative pressure between the intrapleural space and the chest wall, allowing for air to be drawn into the lungs. As children have a very compliant rib cage one of the theoretical ways to improve lung inflation is to apply external pressure on the chest. The intrathoracic pressure increases above atmospheric pressure and air preferentially flows out of the lungs according to the pressure gradient. When the pressure is released and the chest recoils passively, a negative intrathoracic pressure is generated, which allows for air to flow into the lungs according to the pressure gradient created. If a sufficient tidal volume is generated by the release of pressure from the chest this could potentially become a simple, non-invasive, life-saving technique in children with difficult airways. By adapting the principles described above, it is possible that tidal volume and therefore, gas exchange can take place on release of the pressure applied to the chest.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All pediatric patients under the age of 18 years old.
  • All patients requiring a general anesthetic with an endotracheal tube (whether the patient will be intubated with an endotracheal tube will be decided by the anesthesiologist responsible for the case)
  • ASA (American Society of Anesthesiologists Physical Status Classification) I to III

Exclusion criteria

  • Failure to obtain parental consent or patient assent when appropriate (in general children over 8 years old)
  • ASA (American Society of Anesthesiologists Physical Status Classification) IV
  • Patients with any cardiac pathology
  • Patients with any respiratory pathology
  • Patients with any form of chest deformity (examples being pectus excavatum, pectus carinatum, scoliosis)
  • Patients who had previous cardiac/thoracic surgery

Treatment and study plan

Primary outcomes

  1. Tidal volume (mL), as displayed by the Draeger Narkomed 6400 Anesthesia Machine, after release of manual chest compression

    Time frame: After induction of general anesthesia and until completion of surgery (within an average time of 30 mins to 4 hours)

    One tidal volume is displayed on the Draeger machine immediately after the manual release of chest compression. This outcome is recorded 3 times in each patient after fast manual compressions (1-2 seconds each), with the process performed while the patient is both bag-mask ventilated and intubated.

Secondary outcomes

  1. Force of compression (kg), as displayed by the Lafayette Manual Muscle Tester, measured during each manual chest compression

    Time frame: after induction of general anesthesia and during surgery (between 30 mins and 4 hours)

Sponsors and collaborators

Lead sponsor

University of Alberta

Other

Registry information

Official study title

Non-invasive Ventilation Generated by External Chest Pressure in Children

Important dates

Study start
2011
Primary completion
2014
Study completion
2015
First posted
Jul 14, 2011
Registry last updated
Aug 13, 2015

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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