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Trial of Weaning by Synchronized Ventilation

Randomised Trial Comparing Assist Control Ventilation to Pressure Support Ventilation During Weaning

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01376544
Enrollment
36
Registered
2011-06-20
Start date
2008-08-31
Completion date
2010-08-31
Last updated
2011-06-20

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

Conditions

Neonatal Respiratory Failure

Keywords

Neonate, Weaning, Assist control ventilation, Pressure support ventilation

Brief summary

During assist control ventilation and pressure support ventilation (PSV), the start of ventilator inflation is determined by the start of the infant's inspiratory effort. During PSV, termination of inflation is determined by the level of the infant's inspiratory flow. In a randomized trial, no significant differences were found between assist control and pressure support ventilation with regard to the duration of weaning, time to successful extubation, work of breathing, rate of asynchrony and level of respiratory muscle strength.

Detailed description

Objectives: To test the hypothesis that the duration of weaning would be shorter using assist control ventilation (ACV) rather than pressure support ventilation (PSV). To determine if any differences in the duration of weaning reflected differences in the work of breathing, the rate of asynchrony or the level of respiratory muscle strength. Patients and methods: Thirty-six infants, median gestational age 29 (range 24 to 39) weeks, were randomized to weaning by either ACV or PSV. The duration of weaning was recorded. At baseline (study entry), 24 hours after entering the study and immediately prior to extubation, the work of breathing was assessed by measuring the transdiaphragmatic pressure time product (PTPdi), thoracoabdominal asynchrony (TAA) was assessed using respiratory inductance plethysmography and respiratory muscle strength measured by recording the maximal inspiratory pressure produced during an airway occlusion during crying (Pimax). Immediately prior to extubation, the level of active expiration was also assessed.

Interventions

DEVICETreatment protocol designed to evaluate (SLE 5000 ventilator)

Assist control ventilation and pressure support ventilation

Sponsors

King's College London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Days to 14 Days
Healthy volunteers
No

Inclusion criteria

* Ventilated neonates less than 14 days of age

Exclusion criteria

* Congenital heart disease, hypoxic ischaemic encephalopathy

Design outcomes

Primary

MeasureTime frame
To determine which mode of ventilation was associated with a shorter duration of weaning.Up to 28 days after birth

Secondary

MeasureTime frame
Change in Work of breathing thoraco-abdominal asynchrony respiratory muscle strengthBaseline, 24 hours and prior to extubation

Countries

United Kingdom

Outcome results

None listed

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