Actively Recruiting
Genesis Electrical Impedance Tomography (EIT): A Preliminary Study
Led by University of Colorado, Denver · Updated on 2025-11-13
90
Participants Needed
1
Research Sites
391 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to evaluate the Genesis Electrical Impedance Tomography (EIT) imaging system for use in pediatric respiratory disease populations including neuromuscular and bronchopulmonary dysplasia, as well as in age and height matched controls. The EIT does not use radiation, and is read through electrodes.
CONDITIONS
Official Title
Genesis Electrical Impedance Tomography (EIT): A Preliminary Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 2 weeks and 40 years old
- Premature infants older than 2 weeks with confirmed bronchopulmonary dysplasia (BPD) based on NIH criteria
- Chronic respiratory disease due to neuromuscular disease
- Confirmed neuromuscular disease with an echocardiogram done within the last 12 months showing Duchenne muscular dystrophy (DMD) or related mild cardiomyopathy
- Previous ventilation/perfusion (VQ) scan
- Undergoing cardiac catheterization for pulmonary vein stenosis, pulmonary hypertension, or pulmonary artery stenosis
- Healthy controls matched by age and height
You will not qualify if you...
- Younger than 2 weeks old
- Congenital diaphragmatic hernia
- Severe congenital heart disease
- Significant genetic abnormalities
- Conditions interfering with electrode placement on the chest wall
- Unwillingness or refusal to sign consent
- Pregnancy or lactation
- Presence of pacemaker, surgical implant, or spinal implant causing data interference
- Moderate to severe cardiomyopathy
- Temporary cognitive disability due to illness
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Children's Hospital Colorado
Aurora, Colorado, United States, 80045
Actively Recruiting
Research Team
E
Emily DeBoer, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
7
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