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A clinical trial to compare the effects of two methods of oxygen delivery system in children with severe pneumonia requiring oxygen treatment

Clinical effectiveness of Early Humidified High flow Nasal Cannula [HHFNC] oxygen administration method in 2 months to 59 months age group children attending the pediatric emergency room with severe community acquired pneumonia â?? A randomized controlled study - CENTURI Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/04/006788
Enrollment
240
Registered
2016-04-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Pneumonia Health Condition 2: J189- Pneumonia, unspecified organism

Interventions

Intervention1: High Flow Nasal Cannula oxygen administration method: Oxygen will be administered by High flow nasal cannula Control Intervention1: Simple flow nasal cannula oxygen administration metho

Sponsors

INCLEN Trust International
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consecutive children aged 2months to 5 years admitted to pediatric emergency room with severe pneumonia requiring oxygen therapy would be enrolled in this study after getting informed consent from parents

Exclusion criteria

Exclusion criteria: •Children diagnosed to have chronic lung disease •Any child hospitalized for respiratory illness in last one month period •Children previously diagnosed to have bronchial asthma •Children receiving home mechanical ventilation •Children diagnosed to have preexisting neuromuscular disease •Congenital cardiac malformations or other multiple malformations •Children diagnosed to have empyema at admission to emergency room

Design outcomes

Primary

MeasureTime frame
â??Treatment Failureâ?? in 72 hours of hospitalization would be the primary outcome measure and â??Treatment failure" could include any of following (i) Endotracheal intubation, (ii) Mechanical ventilation, (iii) escalating the respiratory support method (using any modality other than primary intervention method)Timepoint: â??Treatment Failureâ?? in 72 hours of hospitalization would be the primary outcome measure and â??Treatment failure" could include any of following (i) Endotracheal intubation, (ii) Mechanical ventilation, (iii) escalating the respiratory support method (using any modality other than primary intervention method)

Secondary

MeasureTime frame
a.Time to clinical stability in hours [Continuous variable] b.Time to respiratory stability in hours [Continuous variable] c.Fluid balance (ml/kg) at 24 and 48 hours of hospitalization [continuous variable] d.Volume of crystalloid bolus requirement [Continuous variable] e.Mortality (In hospital and in 30 days of discharge) [categorical variable] Timepoint: as specified

Countries

India

Contacts

Public ContactK Sasidaran

Dr Mehtas Childrens Hospital, Chennai

sasidarpgi@gmail.com9940587408

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 8, 2026