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A mode of established breathing support versus a mode of established oxygen delivery system in children with an illness of lungs

Noninvasive Ventilation versus Heated Humidified High Flow Nasal Cannula in children with Acute Severe Bronchiolitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047118
Enrollment
116
Registered
2022-11-09
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: J219- Acute bronchiolitis, unspecified

Interventions

Intervention1: NONINVASIVE VENTILATION: NON INVASIVE VENTILATION IS PROVIDED THROUGH DRAGER VENTILATOR MACHINE TILL CLINICAL IMPROVEMENT INTERMS OF REDUCTION OF HEART RATE AND RESPIRATORY RATE AND MA

Sponsors

DR B C ROY POST GRADUATE INSTITUTE OF PEDIATRIC SCIENCES
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The patients aged 1 month to 2 years who are clinically diagnosed as acute severe bronchiolitis according to Modified TAL Score.

Exclusion criteria

Exclusion criteria: 1) Children with congenital diseases like VSD and cardiac failure patients. 2) Emergency need for intubation. 3) Glasgow Coma Scale 4) Hypercapnia (partial pressure of carbon dioxide [PaCO2] >55 mmHg). 5) Cough or gag reflex impairment. 6) Upper airway obstruction. 7) Facial/gastric surgery. 8) Hemodynamic instability. 9) Uncorrected cyanotic congenital heart disease or pulmonary vascular anomalies. 10) Children with respiratory disease other than bronchiolitis like congenital deformity of chest wall or spine or congenital lung malformation. 11) Children with failure to thrive or Protein Energy Malnutrition. 12) Past history of recurrent attacks of respiratory distress with wheezing. 13) Radiological evidence of Pneumonia. 14) Neonates are excluded from the study.

Design outcomes

Primary

MeasureTime frame
cure from disease or need for invasive mechanical ventilationTimepoint: 5 days from initiation of intervention (NIV or HHHFNC)

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactSUBHAJIT BHATTACHARYA

DR.B.C.ROY POST GRADUATE INSTITUTE OF PEDIATRIC SCIENCES

drgm1976@rediffmail.com9836453887

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026