New scanner could replace CT for kids with cystic fibrosis
NCT ID NCT05455671
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether electrical impedance tomography (EIT), a non-invasive imaging technique, can detect lung damage in children and young adults with cystic fibrosis (CF). Researchers compared EIT results to CT scans to see if it can identify air trapping and other lung changes. The study included 48 participants aged 3-21, both healthy and with CF, to see if EIT could monitor disease progression and treatment response without radiation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, EIT could become a safer, radiation-free way to monitor lung health in cystic fibrosis patients, reducing the need for CT scans.
- What could go wrong
- This is a small, early-stage study (48 participants) focused on testing a device's accuracy, not a treatment. It may not prove EIT works better than current methods.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
48 people
The number who actually took part.
- Started
-
Aug 2022
- Finished
-
Aug 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Children and young adults between 3 and 21 years old, with or without cystic fibrosis
- Ages
-
3 to 21 years
- Sex
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Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Cohort 1: * Age 3-21 years * Male or female * Healthy subjects with no known or suspected chronic or temporary lung disease Cohort 2: * Age 3-21 years * Male or female * CF as diagnosed based on sweat chloride value(\>60 mmol/L) or two known disease causing mutations Cohort 3: * Age 3-21 years * Male or female * CF as diagnosed based on sweat chloride value (\>60 mmol/L) or two known disease causing mutations * Experiencing a protocol defined pulmonary exacerbation and being started on oral or intravenous antibiotics Exclusion Criteria: * Unwilling/refusal to sign consent * Known congenital heart disease, arrhythmia, or history of heart failure * Wearing a pacemaker or a metallic surgical implant in the chest * History of infection with Burkholderia cepacia * Developmental delays that could result in an inability to complete study procedures
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Children's Hospital Colorado
Aurora, Colorado, 80045, United States
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