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Clinical Trials/NCT00810459
NCT00810459
Completed
N/A

Trilogy Comparison Study - Pediatrics

Philips Respironics1 site in 1 country6 target enrollmentMarch 10, 2008

Overview

Phase
N/A
Intervention
Not specified
Conditions
Respiratory Failure
Sponsor
Philips Respironics
Enrollment
6
Locations
1
Primary Endpoint
Comparable Level of Gas Exchange for Peripheral Capillary Oxygen Saturation (SpO^2)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The objective of this study (Part II) will be to compare the performance of the Trilogy device and a conventional ventilator (participant's current device). Both devices will be set to the participants' current mode and prescription settings.

Detailed Description

A. Primary Hypothesis and end-point In patients with respiratory insufficiency, when compared to conventional ventilators, the Trilogy device achieves comparable level of gas exchange (measured as partial pressure of carbon dioxide (CO2) in arterial, venous or capillary blood)and peripheral capillary oxygen saturation, (SpO2) levels during various modes of ventilation. B. Secondary Hypothesis and end-points In patients with respiratory insufficiency, when compared to conventional ventilators, the Trilogy device achieves comparable breathing pattern (tidal volume, respiratory rate, minute ventilation), hemodynamics (heart rate), and subjective measures of breathing comfort (measured by modified Borg dyspnea scale).

Registry
clinicaltrials.gov
Start Date
March 10, 2008
End Date
January 26, 2009
Last Updated
5 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age \> 1years of age; \< 18 years of age
  • Greater than 5 kg
  • Considered clinically stable, with low flow oxygen requirements less than 15 LPM (or FIO2 less than 60 %) and PEEP no greater than 10 cm H2O
  • Requiring mechanical ventilation through nasal/facial mask, tracheostomy or endotracheal tube (ET Tube)

Exclusion Criteria

  • Clinically unstable, i.e.,
  • Acute Respiratory Failure
  • Participants with refractory hypotension defined as systolic blood pressure less than 90 mm Hg despite inotropic agents)
  • Uncontrolled cardiac ischemia or arrhythmias
  • or as otherwise determined inappropriate for the study as determined by the investigator
  • Patients suffering from metastatic or terminal cancer and patients with do-not-resuscitate orders

Outcomes

Primary Outcomes

Comparable Level of Gas Exchange for Peripheral Capillary Oxygen Saturation (SpO^2)

Time Frame: After one hour of ventilator use

Comparable level of gas exchange for SpO\^2

Comparable Level of Gas Exchange (Measured as Partial Pressure of Carbon Dioxide (CO2) in Arterial, Venous or Capillary Blood)

Time Frame: After one hour of ventilator use

Comparable level of gas exchange (measured as partial pressure of CO2 in arterial, venous or capillary blood)

Secondary Outcomes

  • Tidal Volume(60 minutes)
  • Heart Rate(60 minutes)
  • Minute Ventilation(60 minutes)

Study Sites (1)

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