Please sign in to follow a disease.
New CT tool aims to sharpen diagnosis of lung fibrosis
NCT ID NCT04676594
First seen Jun 25, 2026 · Last updated Sep 04, 2026 · Updated 4 times
Summary
This study is testing a new tool that uses chest CT scans to help doctors more accurately diagnose different types of pulmonary fibrosis, a lung scarring disease. Researchers will first create the tool by analyzing scans from 300 patients, then test it on 100 additional patients. Three radiologists will read scans with and without the tool to see if it improves their diagnostic accuracy.
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, this tool could help doctors diagnose pulmonary fibrosis more accurately and quickly, leading to better treatment decisions.
- What could go wrong
- This is an observational study using existing scans, not a treatment trial. The tool may not improve accuracy enough to change practice, and results may not apply to all types of fibrosis.
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
-
400 people
The number who actually took part.
- Started
-
Oct 2020
- Expected to finish
-
Aug 2027
An estimate. End dates often move.
- 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
Patients with a diagnosis of usual interstitial pneumonitis, Chronic hypersensitivity pneumonitis or nonspecific interstitial pneumonitis and a chest CT scan.
- Ages
-
21 years and older
- Sex
-
Anyone
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: * Retrospective review of adults (age \> 21) with diagnosis of pulmonary fibrosis on chest CT and a pulmonologist report in electronic medical record confirming the working diagnosis from 1/1/2010 through 7/1/2019. Exclusion Criteria: * Failure to meet inclusion criteria including age \< 21 and lack of a pulmonologists report in the medical record with a working diagnosis of patient's type of pulmonary fibrosis.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Interstitial lung disease are added.
Genom att skicka in godkänner du våra Användarvillkor
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
-
Columbia University Irving Medical Center
New York, New York, 10032, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can Device-Preserved donor lungs boost transplant success?
- Patients and families build a living database of pulmonary fibrosis
- Can better training get doctors to talk about what matters most to dying veterans?
- Inhaled xenon gas could reveal hidden lung vessel disease without catheter
- Radioactive tracer aims to light up hidden lung scarring
- Inhaled drug aims to ease dangerous lung blood pressure in scarred lungs