Lung Diffusing Capacities Normality Thresholds in Pulmonary Fibrosis and Emphysema
NCT ID: NCT07091838
Last Updated: 2025-07-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
120 participants
OBSERVATIONAL
2025-05-13
2025-07-07
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Lung Diffusing Capacity for Nitric Oxide as a Marker of Fibrotic Changes in Idiopathic Interstitial Pneumonias
NCT02596841
Lung Diffusing Capacity for Nitric Oxide and Carbon Monoxide Early After Mild-to-severe COVID-19
NCT04610554
Long COVID and Post-exertional Pulmonary Diffusion
NCT05430503
Assessment of Severity and Prognosis in Elderly Patients With COPD and Complex Chronic Comorbidities
NCT01893918
Mechanisms of Pulmonary Diffusion Limitation in Systemic Sclerosis
NCT03601520
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The choice of reference equations is a crucial issue in the assessment of respiratory function, as it may impact on both definition of normality and assessment of severity. Although for long time the sex-, age- and size-biased percentages of predicted were used for these purposes, the use of z-score is currently recommended as an unbiased estimator of the probability for an individual to deviate from normality. The 5th percentile (-1.645 z-score) of the reference population is currently recommended as the lower limit of normal (LLN5) for all standard lung function measurements including DLco, but for DLNO either LLN5 or the 2.5th percentile (LLN2.5, -1.960 z-score) have been also recommended.
In any case, lung function measures are a continuum and a z-score below a probabilistic threshold such as the LLN5 or LLN2.5 does not necessarily indicate a clinically meaningful abnormality to diagnose a disease but gives the probability of a false positive diagnosis in a healthy subject. By converse, z-scores above these thresholds do not allow to rule out disease with certainty due to the known overlap between healthy and diseased distributions, which may vary depending on various factors including nature and severity of disease, type and method of measures, and reference equations. These proposed limits of normality were based on the distribution in healthy population but not validated for the accuracy to separate diseased from healthy subjects.
The investigators designed the present study with the primary aim to test whether the z-score thresholds of DLco and DLNO separating IPF and PE from healthy subjects may differ from LLN5 or LLN2.5. A secondary aim of the study was to estimate the impact of the choice of test and predicting equations on severity stratification in relation to the extent of lung parenchymal abnormalities typical of IPF and PE. For these purposes, the investigators retrospectively utilized the DLco and DLNO data obtained by a single device in sixty-six subjects with IPF included in two previous studies and in fifty-four new subjects with PE, both documented by quantitative CT of the chest.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Healthy control
Asymptomatic healthy subjects, selected among health professionals and their relatives
No interventions assigned to this group
Interstitial Pulmonary Fibrosis (IPF)
Subjects from investigators' previous studies with interstitial pulmonary fibrosis (IPF), 43 due to usual or nonspecific interstitial pneumonia and 23 to systemic sclerosis
No interventions assigned to this group
Subjects with a smoking history ≥10 pack-years and computed tomography-determined emphysema
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Subjects of white European ancestry with CT-determined IPF and/or PE
Exclusion Criteria
18 Years
85 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
IRCCS Azienda Ospedaliera Universitaria San Martino - IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Giovanni Barisione
Respiratory Pathophysiology Director
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
IRCCS Ospedale Policlinico San Martino
Genova, , Italy
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Zavorsky GS, Hsia CC, Hughes JM, Borland CD, Guenard H, van der Lee I, Steenbruggen I, Naeije R, Cao J, Dinh-Xuan AT. Standardisation and application of the single-breath determination of nitric oxide uptake in the lung. Eur Respir J. 2017 Feb 8;49(2):1600962. doi: 10.1183/13993003.00962-2016. Print 2017 Feb.
Study Documents
Access uploaded study-related documents such as protocols, statistical analysis plans, or lay summaries.
Document Type: Study Protocol
View DocumentOther Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Liguria: 59/2025 - id 14300
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.