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A randomized controlled trial of airway pressure release ventilation and low tidal volume ventilation in pediatric acute respiratory distress syndrome

A randomized controlled trial of airway pressure release ventilation and low tidal volume ventilation in pediatric acute respiratory distress syndrome

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20170320002
Enrollment
14
Registered
2017-03-20
Start date
2017-01-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

pediatric acute respiratory distress syndrome airway pressure release ventilation pediatric acute respiratory distress syndrome airway pressure release ventilation low tidal volume ventilation APRV ARDS

Interventions

mode of ventilator The APRV respiratory cycle is divided into 2 time periods: a longer Thigh period at the higher airway pressure (Phigh) and a much shorter Tlow period during which pressure is releas
controlled and volume&#45
controlled&#44
we use conventional mode in pressure&#45
controlled mode for pediatric acute respiratory distress syndrome with low tidal volume ventilation
Experimental Other,Active Comparator Other
Airway pressure release ventilation,conventional with low tidal volume ventilation

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
1 Months to 15 Years

Inclusion criteria

Inclusion criteria: 1. patients who diagnosed with moderate to severe acute respiratory distress syndrome by definition of The Pediatric Acute Lung Injury Consensus Conference Group (PALICC) 2. patients aged between 1 month - 15 years old 3. all patients were obtained informed consent from parents/ legal representative

Exclusion criteria

Exclusion criteria: 1. congestive heart failure 2. air leak syndrome or preexisting cystic lung disease 3. terminal illness (life expectancy less than 3 months) 4. unstable hemodynamics

Design outcomes

Primary

MeasureTime frame
oxygenation 72 hours PaO2/FiO2

Secondary

MeasureTime frame
all causes of mortality 28 days mortality rate,sedation 7 days total sedation requirement ,28 days - ventilator free day 28 days duration of ventilator free day within 28 days after onset,oxygen index 72 hours mean airway pressure x FiO2/PaO2

Countries

Thailand

Contacts

Public ContactNavaporn Puangpakisiri

King Chulalongkorn Memorial Hospital

navaporn.puang@gmail.com+66-897998787

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026