Using CT scans and biomarkers to improve treatment for pulmonary fibrosis
Official title: The Role of Quantitative CT and Radiomic Biomarkers for Precision Medicine in Pulmonary Fibrosis
Run by University of Virginia · NCT06323876 · Data updated 2026-11-12
This study is testing if special CT scans and biomarkers can help doctors better understand how severe idiopathic pulmonary fibrosis is and how well treatments are working for patients.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 40 Years to 101 Years |
| Sex | All |
| Enrollment | 160 (estimated) |
| Sponsor | University of Virginia Academic / other |
| Locations | 1 site (Charlottesville, Virginia) |
| Status | Recruiting |
| Started | June 20, 2024 |
| Main results expected | May 2028 |
| Study ends | May 2029 |
| Registry record updated | August 16, 2024 |
| Trial ID | NCT06323876 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are individuals aged 40 and older who have been diagnosed with idiopathic pulmonary fibrosis.
✕Probably not a fit
Patients who are pregnant or have significant medical or psychiatric conditions that could affect their safety or ability to complete the study may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to evaluate the role of quantitative CT scans and radiomic biomarkers in assessing disease severity and treatment response in patients with idiopathic pulmonary fibrosis (IPF). Participants will undergo two chest CT scans: a historical baseline scan and a follow-up scan approximately 12 months later. The study seeks to identify and validate radiologic features that can provide insights into disease activity and help guide clinical decision-making. By leveraging advanced imaging techniques, the researchers hope to enhance the understanding of IPF and improve therapeutic strategies.
Why it matters
Potential benefit: If successful, this study could lead to more precise monitoring and treatment strategies for patients with pulmonary fibrosis.
How similar studies have gone: Other studies have shown promise in using advanced imaging techniques and biomarkers for similar conditions, indicating a potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. ≥ 40 years of age 2. Diagnosed with IPF according to 2018 ATS/ERS/JRS/ALAT confirmed by the enrolling investigator 3. Signed informed consent Exclusion Criteria: 1. Pregnancy or planning to become pregnant 2. Women of childbearing potential not willing to remain abstinent (refrain from heterosexual intercourse) or use two adequate methods of contraception, including at least one method with a failure rate of \<1% per year during study participation\* 3. Significant medical, surgical or psychiatric illness that in the opinion of the investigator would affect subject safety or potential to complete the research study * A woman is considered to be of childbearing potential if she is post-monarchical, has not reached a postmenopausal state (≥ 12 continuous months of amenorrhea with no identified cause other than menopause), and has not undergone surgical sterilization (removal of ovaries and/or uterus). Examples of contraceptive methods with a failure rate of \<1% per year include bilateral tubal ligation, male sterilization, established and proper use of hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices.
Where it's running
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University of Virginia
Charlottesville, Virginia, United States Recruiting
Study contacts
- Principal investigator: Noth Imre, MD — Division of Pulmonary and Critical Care
- Study coordinator: Roselove Nunoo-Asare
- Email: rnn3b@uvahealth.org
- Phone: 4342436074
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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New IPF drug ORJ-001 tested in adults with IPF
A phase 2 study tests ORJ-001 versus placebo in adults with idiopathic pulmonary fibrosis to see if it is tolerated and whether it helps lung function.
-
Nalbuphine ER for IPF-related chronic cough
This study tests whether extended-release nalbuphine tablets can reduce chronic cough in people with idiopathic pulmonary fibrosis.
-
Inspiratory Flow Rate Capability in Pulmonary Fibrosis Patients
This observational study tests how fast patients with IPF or PPF can inhale through dry powder inhalers with different resistances.
-
Photon-counting CT vs standard HRCT to help diagnose IPF and other ILDs
This study tests whether photon-counting CT can improve identifying IPF and other ILDs compared with standard HRCT for patients discussed in multidisciplinary teams.
-
Rentosertib by mouth for people with idiopathic pulmonary fibrosis
This is a randomized, placebo-controlled test to see if Rentosertib helps adults with idiopathic pulmonary fibrosis when taken as a pill.
-
Inhaled nintedanib powder for IPF in adults
This study tests whether an inhaled form of nintedanib can safely help adults with idiopathic pulmonary fibrosis.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.