MedPath

Continuous Regional Analysis Device for neonate Lung (CRADL)

Completed
Conditions
respiratory failure
10028971
Registration Number
NL-OMON46059
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
125
Inclusion Criteria

Age less than 7 years (limited by available electrode belt sizes)
Admitted to the NICU or the PICU
At high risk of or developing respiratory failure for which respiratory support is needed
Written informed consent from both parents or legal representatives

Exclusion Criteria

Postmenstrual age < 25 weeks
Birth weight < 600 g
Electrical active implant
Chest skin lesions preventing placement of electrode belt

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Distribution of tidal ventilation before and after an intervention or event<br /><br>that is know for its changes in regional lung aeration and the regional changes<br /><br>in the right vs the left lung and the anterior vs the posterior part of the<br /><br>lung. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>The relationship and timing of EIT changes compared with onset of<br /><br>intervention/event or the results from other diagnostic tools will be explored.</p><br>
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