Validation of clinical applicable techniques for end inspiratory lung volume (Vei) measurement.

Validation of clinical applicable techniques for end inspiratory lung volume (Vei) measurement. - Vei measurement

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON42776

Enrollment

Registered

2015-09-23

Start date

2015-11-18

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

pulmonary hyperinflation too high lung volume

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - severe airway obstruction due to obstructive airway diseases ( COPD and asthma) - controlled mechanical ventilation - deep sedation - arterial catheter

Exclusion criteria

Exclusion criteria: - hypoxemic failure (FiO2 > 70%) - presence of pneumothorax

Design outcomes

Primary

Measure	Time frame
The primary study parameter is the difference in degree of pulmonary hyperinflation, expressed as the volume at end inspiration (Vei) between the gold standard and formula (Vei_measurement versus Vei_formula) and between the gold standard and the ventilator (Vei_measurement versus Vei_ventilator).	—

Secondary

Measure	Time frame
Other study parameters are based on clinical outcome of patients, such as incidence of pneumothorax, days on the ventilator and need for vasopressors.	—

Countries

Netherlands

Outcome results