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Clinical Trials/NCT02948530
NCT02948530UnknownNot Applicable

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

Stefan Lundin1 site in 1 country30 target enrollmentStarted: October 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Measurement of lung elastance and transpulmonary pressure

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Case Crossover
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Mechanically ventilated patients in the intensive care unit

Exclusion Criteria

  • Patients with chronic obstrucive lung disease

Outcomes

Primary Outcomes

Measurement of lung elastance and transpulmonary pressure

Time Frame: Within one hour

Comparison of a new versus the classical method for measurement of transpulmonary pressure

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Stefan Lundin
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Stefan Lundin

Professor

Sahlgrenska University Hospital, Sweden

Study Sites (1)

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