Skip to content

Effect of balloon volume on oesophageal pressure monitoring in critically ill children: a pilot study

Effect of balloon volume on oesophageal pressure monitoring in critically ill children: a pilot study - Balloon volume and Poes

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON44610
Enrollment
50
Registered
2018-01-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Lung injury

Interventions

Insertion esophageal cathether
Balloon volume
Mechanical ventilation
Oesophageal pressure

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
2 Years to 11 Years

Inclusion criteria

Inclusion criteria: * Informed consent * Age younger than 12 years * Need for mechanical ventilation with PEEP >

Exclusion criteria

Exclusion criteria: No informed consent * Chronic respiratory failure on home ventilation * Intracranial hypertension * Bone marrow transplantation * Immunocompromised patients (congenital or acquired) * Pre-existing pulmonary hypertension * Uncorrected congenital heart disease with left * to * right shunting or cyanotic heart disease * Single ventricle laesions * Evidence of esophageal pathology or the inability to pass a combined esophageal balloon/nasogastric feeding tube * Contraindication to the passage of an esophageal pressure probe by either the oral or nasal route * Withdrawal of life * sustaining treatment

Design outcomes

Primary

MeasureTime frame
Peak-to-through oesophageal pressure at varying amounts of air in balloon

Secondary

MeasureTime frame
Peak-to-through oesophageal pressure at varying amounts of air in balloon and body position (supine vs 30° upright

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)