search
Back to results

Home Oxygen Therapy in Bronchiolitis (O2-Rx)

Primary Purpose

Bronchiolitis

Status
Unknown status
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Oxygen Therapy
Sponsored by
Meir Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Bronchiolitis focused on measuring Bronchiolitis, Infants, Nebulized Inhalation, RSV, Oxygen

Eligibility Criteria

8 Weeks - 24 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants, aged less than 24 months treated for acute viral bronchiolitis in a pediatric ambulatory clinic in central Israel, during the winter season (December through April) of 2011-2013. The clinical diagnosis will be based on findings of a first clinical bronchiolitis requiring oxygen for hypoxia.

Exclusion Criteria:

  • Infants with chronic diseases, such cardiorespiratory disease, cystic fibrosis or neonatal asthma, malignancy or immunodeficiency will be excluded, as will be infants in severe distress (respiratory rate >80breaths/min, heart rate >200beats/min, BCD score >13, SpO2). Infants who had recovered from chronic neonatal lung disease of prematurity will be included. In addition, we will excluded infants who had received corticosteroids or bronchodilators in any form within 14 days before presentation and infants whose parents refused to participate or were unable to complete the Bronchiolitis Caregiver Diary Score.

Sites / Locations

  • Gani- Hdar Clinic
  • Clalit health services -Gani Hadar Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

hypertonic inhalation + O2

Epinephrine & bromhexine nebulized + O2

Arm Description

oxygen for 30 minuets after inhalation of 3% saline 4 times daily

oxygen for 30 minuets after inhalation of racemic epinephrine with bromhexine 4 times daily

Outcomes

Primary Outcome Measures

Home oxygen therapy in the ambulatory treatment of bronchiolitis
Primary outcome measures of the study will be the number of emergency room visits or hospitalizations within two weeks of enrollment in the study.

Secondary Outcome Measures

Home oxygen therapy in the ambulatory treatment of bronchiolitis
Secondary outcome measures the change in bronchiolitis caregiver diary (BCD) score.
daycare(patients) and work (parents) lost because of the illness.
Number of day that patient has missed from daycare, forcing one parent to miss work

Full Information

First Posted
October 6, 2010
Last Updated
July 10, 2011
Sponsor
Meir Medical Center
search

1. Study Identification

Unique Protocol Identification Number
NCT01216553
Brief Title
Home Oxygen Therapy in Bronchiolitis
Acronym
O2-Rx
Official Title
Home Oxygen Therapy in the Ambulatory Treatment of Bronchiolitis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2011
Overall Recruitment Status
Unknown status
Study Start Date
October 2011 (undefined)
Primary Completion Date
May 2013 (Anticipated)
Study Completion Date
August 2014 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Meir Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study was to investigate the utility and safety of home management of home oxygen therapy in acute bronchiolitis. A matched case-control study, of one hundred and thirty five infants aged less than 12 months diagnosed bronchiolitis with hypoxia attending a pediatric community clinic will be randomly assigned to receive oxygen with or without standard nebulized therapy. Nebulized treatment with either 0.1% epinephrine diluted in bromhexine, or 3% hypertonic saline. Intermittent oxygen treatment will be administered 6 times daily for 7 days. Primary outcome measures will be emergency department visits/hospitalization secondary outcome measures will be changes in Bronchiolitis Caregiver Diary Score.
Detailed Description
Bronchiolitis is an infection of the bronchiolar epithelium. It is associated with profound submucosal and adventitial edema, increased secretion of mucus, and obstructed flow in the small airways, leading to hyperinflation, atelectasis, and wheezing. Respiratory syncytial virus (RSV) is responsible for the majority of cases .Bronchiolitis is the most frequent lower respiratory tract infection with high morbidity, and the leading cause of hospitalization in young children. Studies from developed countries report an incidence hospitalization of 30 per 1000 children in the first year of life and an annual mortality rate of 1.82-2 per 100,000 live births. The cost of treatment is about $2.5 billion yearly. One group from the United States estimated the annual hospital costs for bronchiolitis at $365-$691 million. Of children who develop bronchiolitis during the first 2 year of life, approximately 1 in 10 ( 3% of all infants in the USA) will be hospitalized furthermore, a substantial proportion of infants remain in the hospital to receive oxygen until their hypoxia has improved. The current in hospital treatment for acute viral bronchiolitis is mainly supportive, consisting of supplemental oxygen, suction and hydration . Airway edema and sloughing of respiratory epithelia cell cause mismatching of ventilation and perfusion and subsequently reduction in oxygenation (PaO2 and Spo2). Emergency Department referral (ED) and Hospital admission (HA) admission, have increased secondary to increase sensitivity of pulse oximetry for detection of hypoxia ( compared with clinical observation. The therapeutic role of bronchodilators although of questionable clinical importance is commonly used A recent review reported has shown short-term improvement in clinical scores, but no improvement in oxygenation or rate of hospitalization. Neither systemic glucocorticoids nor antibiotics appear to have any clinically significant effect on the disease course. Antiviral agents (Ribavirin) are indicated only in children with a serious underlying disorder. Trials with chest physiotherapy using vibration and percussion techniques failed to reduce the severity of the illness, length of hospitalization, or oxygen requirements, and treatment with nebulized furosemide ,inhaled interferon alpha-2a (Roferon A) ,and rhDNase proved ineffective. Clinicians are now influenced significantly in their decision for Emergency Department referral and hospitalization of patient with respiratory disease. We hypothesized that adding short term home intermittent oxygen therapy for 7 days to other treatment modalities will reduce hypoxias and Emergency Ward referral. The aim of the present study was to compare the outcome of this combined treatment with oxygen with other medical modalities to oxygen alone and with placebo in children with RSV bronchiolitis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchiolitis
Keywords
Bronchiolitis, Infants, Nebulized Inhalation, RSV, Oxygen

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
135 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
hypertonic inhalation + O2
Arm Type
Active Comparator
Arm Description
oxygen for 30 minuets after inhalation of 3% saline 4 times daily
Arm Title
Epinephrine & bromhexine nebulized + O2
Arm Type
Active Comparator
Arm Description
oxygen for 30 minuets after inhalation of racemic epinephrine with bromhexine 4 times daily
Intervention Type
Other
Intervention Name(s)
Oxygen Therapy
Other Intervention Name(s)
O2
Intervention Description
1 lt/min oxygen via nasal cannulae intermittently for 30 minuets 4 times daily for 7 days
Primary Outcome Measure Information:
Title
Home oxygen therapy in the ambulatory treatment of bronchiolitis
Description
Primary outcome measures of the study will be the number of emergency room visits or hospitalizations within two weeks of enrollment in the study.
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Home oxygen therapy in the ambulatory treatment of bronchiolitis
Description
Secondary outcome measures the change in bronchiolitis caregiver diary (BCD) score.
Time Frame
1 month
Title
daycare(patients) and work (parents) lost because of the illness.
Description
Number of day that patient has missed from daycare, forcing one parent to miss work
Time Frame
1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Weeks
Maximum Age & Unit of Time
24 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants, aged less than 24 months treated for acute viral bronchiolitis in a pediatric ambulatory clinic in central Israel, during the winter season (December through April) of 2011-2013. The clinical diagnosis will be based on findings of a first clinical bronchiolitis requiring oxygen for hypoxia. Exclusion Criteria: Infants with chronic diseases, such cardiorespiratory disease, cystic fibrosis or neonatal asthma, malignancy or immunodeficiency will be excluded, as will be infants in severe distress (respiratory rate >80breaths/min, heart rate >200beats/min, BCD score >13, SpO2). Infants who had recovered from chronic neonatal lung disease of prematurity will be included. In addition, we will excluded infants who had received corticosteroids or bronchodilators in any form within 14 days before presentation and infants whose parents refused to participate or were unable to complete the Bronchiolitis Caregiver Diary Score.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
E. Michael sarrell, MD
Phone
+972-544-289279
Email
michaelsar@clalit.org.il
Facility Information:
Facility Name
Gani- Hdar Clinic
City
Petah Tiqwa
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
E. Michae sarrell, MD
Phone
+972-544-289279
Email
michaelsar@clalit.org.il
First Name & Middle Initial & Last Name & Degree
E. Michael Sarrell, MD
Facility Name
Clalit health services -Gani Hadar Clinic
City
Tel Aviv
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
e. michael sarrell, md
Phone
+972-544-289279
Email
michaelsar@clalit.org.il
First Name & Middle Initial & Last Name & Degree
E. MICHAEL SARRELL, MD

12. IPD Sharing Statement

Learn more about this trial

Home Oxygen Therapy in Bronchiolitis

We'll reach out to this number within 24 hrs