- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02948530
Measurement of Lung Elastance and Transpulmonary Pressure Using Two Different Methods (Lungbarometry)
Study Overview
Status
Conditions
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 Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Stefan Lundin, MD, PhD
- Phone Number: +46313428112
- Email: stefan.lundin@gu.se
Study Contact Backup
- Name: Magni Gudmundsson, MD
- Phone Number: +46 31 3421000
- Email: magni.gudmundsson@vgregion.se
Study Locations
-
-
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Gothenburg, Sweden, S-413 45
- Recruiting
- Sahlgrenska University Hospital
-
Contact:
- Stefan Lundin, MD PhD
- Phone Number: +46 708744379
- Email: stefan.lundin@gu.se
-
Sub-Investigator:
- Magni Gudmundsson, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Mechanically ventilated patients in the intensive care unit
Exclusion Criteria:
Patients with chronic obstrucive lung disease
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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
|
Within one hour
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Stefan Lundin, MD, PhD, Sahlgrenska University Hospital, Sweden
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LUA-74204
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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