MedTrace Logo

Trilogy Comparison Study - Pediatrics

NCT00810459 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2021-02-03

Study results available
· View outcomes & findings →

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.

Conditions

Interventions

DEVICE

Trilogy Ventilator

Exposure to one hour on the Trilog ventilator

DEVICE

Standard of Care

Exposure of one hour on the Participants prescribed ventilator

Sponsors & Collaborators

  • Philips Respironics

    lead INDUSTRY

Principal Investigators

  • Steven Mink, MD · University of Manitoba

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
1 Year
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-10
Primary Completion
2009-01-26
Completion
2009-01-26
FDA Device
Yes

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00810459 on ClinicalTrials.gov