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New scanner could replace CT for kids with cystic fibrosis

NCT ID NCT05455671

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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

More trials for these conditions

Other studies related to the condition(s) this trial covers.