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Study of High-flow Oxygen Therapy Against Standard Therapy in Bronchiolitis (Hi-Flo)

Primary Purpose

Bronchiolitis

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
High Flow Nasal Cannula Oxygen Therapy
Standard low flow oxygen
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bronchiolitis focused on measuring Bronchiolitis, High, Flow, Oxygen, Therapy, Nasal, Cannulae, Prongs

Eligibility Criteria

undefined - 18 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All children under 18 months of age with a clinical diagnosis of bronchiolitis requiring admission to hospital for observation and oxygen.

Exclusion Criteria:

  • Infants admitted directly to ICU from Emergency.
  • Prior positive pressure home ventilation.
  • Tracheostomy.
  • Nasogastric tubes in situ on admission.
  • Upper airway abnormality.
  • Congenital heart disease.

Sites / Locations

  • British Columbia Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control

Intervention

Arm Description

Standard low-flow oxygen therapy.

High Flow Nasal Cannula Oxygen Therapy

Outcomes

Primary Outcome Measures

Length of hospital stay
Number of hours that the patient remains in hospital.

Secondary Outcome Measures

Admission to Intensive Care Unit
Yes or No
Work of breathing
Work of breathing, assessed by respiratory rate, at four timepoints on day one, and daily thereafter

Full Information

First Posted
December 16, 2011
Last Updated
May 8, 2015
Sponsor
University of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT01498094
Brief Title
Study of High-flow Oxygen Therapy Against Standard Therapy in Bronchiolitis
Acronym
Hi-Flo
Official Title
A Prospective Open Randomized Clinical Trial Comparing High Flow Nasal Cannula Oxygen Therapy Against Standard Therapy for Children Hospitalized With Bronchiolitis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
December 2011 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of British Columbia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Bronchiolitis is a common illness of the respiratory tract caused by infection of the tiny airways within the lungs called bronchioles. At present the standard care of hospitalized children with bronchiolitis is oxygen via nasal prongs. In this study the investigators would like to compare standard ward management with a new method of delivering oxygen called high flow nasal cannula oxygen therapy (HFNOT). HFNOT involves breathing warmed, moistened oxygen through nasal cannulae at a flow rate of 8 liters/minute. Accumulated experience suggests that HFNOT eases the child's work of breathing and reduces need for ICU admission and invasive respiratory support.
Detailed Description
We propose a prospective open randomised controlled trial to compare high flow nasal cannula oxygen therapy (HFNOT) with standard oxygen therapy for infants hospitalised with bronchiolitis. This study will be the first of its kind, as currently there is no evidence in the published literature. All children will be cared for by the same medical team on two wards. All aspects of care other than oxygen delivery will not be specified, and be at the discretion of the physicians. HFNOT will not be used as an escalation of care on the wards. Randomisation will be performed by REDcap, in blocks of 6 patients. Patients will be identified in Emergency, informed consent obtained, and treatment started prior to transfer to the ward. For patients randomised to HFNOT, the flow rate will be fixed at 8 liters/minute, and the inspired oxygen concentration titrated to maintain saturations above 92%. Interim statistical analysis will be conducted to determine any positive or negative effect of HFNOT therapy. The first interval analysis will be performed after 50 subjects, the second after 100 subjects. If an effect is found, the study will be terminated following discussion with the hospital statistician and ethics board. Whichever treatment arm is found to be beneficial will be instituted as standard care for children with bronchiolitis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchiolitis
Keywords
Bronchiolitis, High, Flow, Oxygen, Therapy, Nasal, Cannulae, Prongs

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
79 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Active Comparator
Arm Description
Standard low-flow oxygen therapy.
Arm Title
Intervention
Arm Type
Experimental
Arm Description
High Flow Nasal Cannula Oxygen Therapy
Intervention Type
Procedure
Intervention Name(s)
High Flow Nasal Cannula Oxygen Therapy
Other Intervention Name(s)
High flow oxygen therapy
Intervention Description
Warm humidified oxygen will be delivered at 8 liters/minute via nasal cannulae, at a concentration that maintains saturations greater than 92%.
Intervention Type
Other
Intervention Name(s)
Standard low flow oxygen
Intervention Description
Standard low flow oxygen will be given to patients to maintain saturations greater than 92%.
Primary Outcome Measure Information:
Title
Length of hospital stay
Description
Number of hours that the patient remains in hospital.
Time Frame
Expected average length of stay 5 days
Secondary Outcome Measure Information:
Title
Admission to Intensive Care Unit
Description
Yes or No
Time Frame
During hospitalisation for bronchiolitis, expected average 5 days
Title
Work of breathing
Description
Work of breathing, assessed by respiratory rate, at four timepoints on day one, and daily thereafter
Time Frame
During hospital stay, expected average 5 days

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All children under 18 months of age with a clinical diagnosis of bronchiolitis requiring admission to hospital for observation and oxygen. Exclusion Criteria: Infants admitted directly to ICU from Emergency. Prior positive pressure home ventilation. Tracheostomy. Nasogastric tubes in situ on admission. Upper airway abnormality. Congenital heart disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Wensley, MD
Organizational Affiliation
British Columbia Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
British Columbia Children's Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6H 3N1
Country
Canada

12. IPD Sharing Statement

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Study of High-flow Oxygen Therapy Against Standard Therapy in Bronchiolitis

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