Clinical Trials Directory

Trials / Completed

CompletedNCT02290535

Electrical Impedance Tomography of Lung in Child and Young Age

Status
Completed
Phase
Study type
Observational
Enrollment
192 (actual)
Sponsor
RWTH Aachen University · Academic / Other
Sex
All
Age
5 Years – 18 Years
Healthy volunteers
Accepted

Summary

The investigator will determine a compliance of two diagnostic techniques (EIT and Body plethysmography) in collective of children and teenagers with obstructive lung disease and a matched control group.

Detailed description

The aim of the present study is verification of the correlation between EIT-derived data and following extracted parameters of the pulmonary function: * forced expiratory volume in 1 second (FEV 1) * forced vital capacity (FVC) * relative forced expiratory volume in 1 second (FEV1/FVC) * maximal expiratory flow (MEF 25) * total lung capacity (TLC) * resistance (Raw). These findings could bring out new prospective opportunity for pulmonary function tests without cooperation. Furthermore, the study aims to clarify whether EIT technique can be used for regional pulmonary function testing. In addition, dynamic lung function parameter and static radiological techniques will be correlated with EIT.

Conditions

Interventions

TypeNameDescription
PROCEDUREpatientsThe 16-electrode belt will be applied to patient's chest. Following vital signs will be recorded: respiratory rate at rest breathing, heart rate, transcutaneous oxygen saturation. Then impulse oscillometry (IOS) will be performed in a sitting position. After that, subjects with cooperation willingness will get a body plethysmography. A spirometry / forced breathing maneuvers will be performed. All patients will receive 2 strokes salbutamol inhaler for bronchospasmolysis. Please note that inhalation of salbutamol is not study related. It is used in the clinical routine to examine the reversibility of the bronchial obstruction in patients with obstructive lung disease in course of the lung function test. Ten minutes later measurements described above will be repeated.
PROCEDUREprobandsProbands will receive the same treatment as patients, but without bronchospasmolysis.

Timeline

Start date
2014-06-01
Primary completion
2015-01-01
Completion
2015-01-01
First posted
2014-11-14
Last updated
2015-07-16

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02290535. Inclusion in this directory is not an endorsement.