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High Flow Nasal Cannula Therapy in Bronchiolitis : Early vs Rescue

Heated Humidified High Flow Nasal Cannula (HHHFNC) For Acute Moderate to Severe RSV-Bronchiolitis in Infants Younger Than 3 Months Old: Early Versus Rescue

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03095495
Enrollment
28
Registered
2017-03-29
Start date
2018-08-14
Completion date
2024-05-28
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchiolitis, Respiratory Syncytial Virus (RSV)

Keywords

Heated Humidified High Flow Nasal Cannula (HHHFNC), Low Flow Nasal Cannula, Bronchiolitis, Respiratory Syncytial Virus (RSV), Respiratory Failure, High Flow Nasal Cannula (HFNC), Lung Diseases, Obstructive

Brief summary

The enrolled RSV-bronchiolitis patients will be randomized into two arms , the early HHHFNC group and the standard therapy group with rescue HHHFNC to study the efficacy of this treatment.

Detailed description

Setting: The study will be conducted between June 2017 and June 2020 in the short stay unit of the Pediatric Emergency Center (PEC) of Hamad General Hospital, the only pediatric emergency facility in the State of Qatar. Infants aged ≤3 months presenting to the unit for treatment of viral bronchiolitis with positive RSV test will be eligible for the study. Procedure: Eligible patients will be enrolled after obtaining written consent. For patients who consent, plain chest radiography, and nasopharyngeal swabs will be taken for RSV detection. If the patient has a positive RSV rapid antigen test, patients will be randomized in one of the study arms. Adverse effects in each group will be carefully monitored and documented. Study Intervention: Patients will be randomized into two treatment arms Group 1: Early HHHFNC Group Patients in this group will be treated by using heated humidified high flow oxygen /air via nasal cannula; investigators will keep the patient on HHHFNC until he/she becomes clinically ready for discharge. Group 2: Standard Therapy and Rescue HHHFNC Group: patients in this group will be treated by usual therapy,investigators will use low flow nasal cannula oxygen therapy only if oxygenation needed to maintain Oxygen saturation (SpO2) ≥ 92% , if the patient deteriorate and require ICU, rescue HHHFNC will be started before admission to the ICU.

Interventions

HHHFNC therapy is a simple to use system that delivers warm and moist air/oxygen mixture at high flow rates that generate positive airway pressure

DEVICEStandard Therapy (Low Flow Nasal Cannula)

will be used only if the patient needs oxygenation and Rescue HHHFNC will be used if the patient needs PICU

Sponsors

Sidra Medicine
CollaboratorOTHER
Hamad Medical Corporation
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 3 Months
Healthy volunteers
No

Inclusion criteria

* Previously healthy infants with age 0-3 months and gestational age ≥30 weeks admitted to the short stay unit with RSV positive bronchiolitis and clinical severity score ≥4 on Wang clinical severity scale.

Exclusion criteria

1. Gestational age less than 30 weeks. 2. Previous history of wheezing. 3. Use of steroid within 48 hours of presentation. 4. History of chronic lung disease. 5. Infants admitted directly to ICU. 6. Prior invasive or non-invasive ventilatory support. 7. Tracheostomy. 8. Nasogastric tubes in situ on admission. 9. Upper airway abnormality (like choanal atresia and midfacial anomalies). 10. Immunodeficient children. 11. History of cardiac disease, renal disease or liver disease. 12. History of neuromuscular disorder.

Design outcomes

Primary

MeasureTime frameDescription
The rate of Pediatric Intensive Care Unit (PICU) admissionsThrough study completion, an average of 3 yearThe rate of Pediatric Intensive Care Unit admissions

Secondary

MeasureTime frameDescription
Mean length of stay (LOS)Through study completion, an average of 3 yearGeometric mean length of stay in the short stay unit
Bronchiolitis Severity Score (BSS)Up to 72 hoursBronchiolitis Severity Score at 4, 8, 12, 24, 36, 48, 72 hours
Percentage of revisit, infirmary short-stay and admission to the hospital or PICU2 weeks after dischargePercentage of revisit, infirmary short-stay and admission to the hospital or PICU for the same illness on follow up for two weeks post discharge
Transcutaneous Partial Pressure of Carbon Dioxide (PtcCO2)Up to 72 hoursTranscutaneous Partial Pressure of Carbon Dioxide (PtcCO2) at 4,8,12,24,36,48,72 hours
Percentage of patients who are on the standard therapy arm and required ICU admission, but improved after the rescue HHHFNC in the ED1 hour after starting of rescue HHHFNCPercentage of patients who are on the standard therapy arm and required ICU admission, but improved after the rescue HHHFNC in the ED

Countries

Qatar

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026