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Measurement of Lung Elastance and Transpulmonary Pressure Using Two Different Methods (Lungbarometry)

Measurement of Lung Elastance and Transpulmonary Pressure Using Two Different Methods (Lungbarometry)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02948530
Enrollment
30
Registered
2016-10-28
Start date
2016-10-31
Completion date
2018-12-31
Last updated
2018-04-11

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

Conditions

Acute Lung Injury

Brief summary

Classically lung elastance and transpulmonary pressure are measured from the difference in tidal variations of airway pressure subtracted by tidal variations i esophagus pressure divided by the tidal volume. This requires the presence of a esophageal balloon catheter which is cumbersome and costly. In this study values obtained as described above are compared to values obtained with a new method in which a stepwise increase in positive endexpiratory pressure (PEEP) is performed with a size of the lung volume increase which corresponds to the tidal volume which the patient is ventilated with. The measurements are performed in sedated and mechanically ventilated patients in the intensive care unit.

Detailed description

Classically lung elastance and transpulmonary pressure are measured from the difference in tidal variations of airway pressure subtracted by tidal variations in esophageal pressure divided by the tidal volume (Method 1). This requires the presence of a esophageal balloon catheter which is cumbersome and costly. In this study values obtained as described in Method 1 above are compared to values obtained with a new method (Method 2) in which a PEEP-step is performed with a size of the lung volume increase which corresponds to the tidal volume which the patient is ventilated with. Measurements using Method 1 and 2 are performed in sedated and mechanically ventilated patients in the intensive care unit.

Interventions

None listed

Sponsors

Stefan Lundin
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Mechanically ventilated patients in the intensive care unit

Exclusion criteria

Patients with chronic obstrucive lung disease

Design outcomes

Primary

MeasureTime frameDescription
Measurement of lung elastance and transpulmonary pressureWithin one hourComparison of a new versus the classical method for measurement of transpulmonary pressure

Countries

Sweden

Contacts

Primary ContactStefan Lundin, MD, PhD
stefan.lundin@gu.se+46313428112
Backup ContactMagni Gudmundsson, MD
magni.gudmundsson@vgregion.se+46 31 3421000

Outcome results

None listed

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