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Clinical Trials/NCT03309085
NCT03309085
Completed
Not Applicable

Functional Imaging With Computational Fluid Dynamics to Evaluate the Airways in Patients With Acute Lung Injury

University Hospital, Antwerp1 site in 1 country7 target enrollmentAugust 13, 2013
ConditionsARDS, Human

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
ARDS, Human
Sponsor
University Hospital, Antwerp
Enrollment
7
Locations
1
Primary Endpoint
Regional bronchial recruitment
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This is a prospective single-center cohort trial to compare regional bronchial recruitment, bronchial distention and alveolar recruitment in 6 patients with acute respiratory distress syndrome (ARDS). The investigators used CT scan images as the imaging modality, and the subjects were scanned on end-expiratory lung volume with different positive end-expiratory pressures. Those images were post-processed to evaluate the airways.

Registry
clinicaltrials.gov
Start Date
August 13, 2013
End Date
April 14, 2014
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tom Schepens, MD

Research fellow

University Hospital, Antwerp

Eligibility Criteria

Inclusion Criteria

  • mechanically ventilated
  • moderate or severe ARDS, as defined by the Berlin criteria

Exclusion Criteria

  • pregnancy
  • hemodynamic instability
  • obesity (BMI \>30)

Outcomes

Primary Outcomes

Regional bronchial recruitment

Time Frame: Through study completion, within 24 hours after inclusion

The difference in bronchial tree volume increase from one PEEP level to the other

Regional bronchial dilation

Time Frame: Through study completion, within 24 hours after inclusion

The difference in bronchial diameter from one PEEP level to the other

Regional alveolar recruitment

Time Frame: Through study completion, within 24 hours after inclusion

The difference in alveolar volume from one PEEP level to the other

Secondary Outcomes

  • Correlation between parenchymal recruitment and bronchial recruitment(Through study completion, within 24 hours after inclusion)

Study Sites (1)

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