A blood test that could predict who survives a lung disease crisis?
NCT ID NCT07783230
First seen Aug 24, 2026 · Last updated Aug 25, 2026 · Updated 1 time
Summary
This study looks at whether routine blood tests can help predict how patients with a sudden worsening of idiopathic pulmonary fibrosis (IPF) will fare. Researchers will track blood cell ratios and oxygen levels in hospitalized patients over two weeks. The goal is to see if changes in these simple markers can signal who might need more aggressive treatment early on.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- No drug or intervention is being tested; this is an observational study using routine blood tests (complete blood count-derived inflammatory indexes) as potential biomarkers.
- What this could lead to
- If successful, this could give doctors a simple, low-cost way to identify which patients with acute IPF exacerbations need more intensive care early on.
- What could go wrong
- This is a small, observational study, so the findings may not apply to all patients. The blood tests are not proven predictors yet and need validation in larger groups.
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
-
About 70 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Sep 2026
An estimate. Start dates often move.
- Expected to finish
-
Oct 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
The study population consists of adult patients (18 years of age or older) with an established diagnosis of idiopathic pulmonary fibrosis (IPF) who are admitted to a tertiary referral center (Assiut University Hospitals) for an acute exacerbation of IPF within 72 hours of symptomatic worsening.
- Ages
-
18 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: * Age 18 years or older. * Established diagnosis of idiopathic pulmonary fibrosis per the 2023 ATS/ERS/JRS/ALAT clinical practice guideline, based on a multidisciplinary assessment incorporating clinical features, high-resolution computed tomography pattern, and, where available, surgical lung biopsy. * Hospital admission for acute exacerbation of IPF meeting the 2016 International Working Group criteria: previous or concurrent IPF diagnosis; acute worsening or development of dyspnea of less than one month duration; computed tomography showing new bilateral ground-glass abnormality or consolidation superimposed on a background pattern of usual interstitial pneumonia; deterioration not fully explained by cardiac failure or fluid overload and triggered exacerbations would be included. * Admission within 72 hours of symptomatic worsening. * Written informed consent from the patient or legally authorized representative. Exclusion Criteria: * Alternative explanation for acute respiratory deterioration confirmed at or shortly after admission, including but not limited to microbiologically confirmed bacterial pneumonia with positive blood or respiratory culture, computed-tomography-confirmed pulmonary embolism, cardiogenic pulmonary edema with elevated brain natriuretic peptide and supportive echocardiographic findings, or pneumothorax. * Interstitial lung disease attributable to a defined cause: connective-tissue-disease-associated ILD, chronic hypersensitivity pneumonitis, occupational pneumoconiosis, sarcoidosis, or drug-induced ILD. * Active solid or hematologic malignancy, including any malignancy under active treatment within the preceding 12 months. * Receipt of cytotoxic chemotherapy, radiotherapy, or non-IPF immunosuppressive therapy (excluding maintenance corticosteroid at prednisolone-equivalent $\\le$ 10 mg daily) within the preceding 30 days. * Primary hematologic disorder altering the complete blood count, including leukemia, lymphoma, myelodysplastic syndrome, aplastic anemia, or known immune-mediated cytopenia. * Anticipated transfer to another facility within 72 hours of admission.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Acute exacerbation of idiopathic pulmonary fibrosis are added.
By submitting, you agree to our Terms of use
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a thousand patient records unlock better care for a rare lung disease?
- Sharper CT scans may solve a lung disease diagnostic puzzle
- Can we untangle the overlap of lung diseases? a new study aims to find out
- Can a new pill slow lung scarring in IPF?
- Beyond the lungs: the hidden emotional toll of IPF medications
- Can umbilical cord stem cells ease a scarring lung disease?