CT Quantitative Assessment of Interstitial Lung Disease
Interstitial Lung Disease
What this study involves
The registry does not currently label this study as recruiting. Ask about its status before planning a screening visit.
- Study type
- Observational
- Phase
- Not applicable / not listed
- Age range
- 18 years - 90 years
- Sex eligible
- All sexes
- Healthy volunteers
- Not accepted
- Participants
- 70 Estimated
These are starting points, not an eligibility decision. The research team must review the full requirements.
About the research
Interstitial lung disease (ILD) refers to a broad category of heterogeneous lung diseases with different etiologies and features characterized by inflammation and fibrosis of the lung parenchyma and manifested as exertional dyspnea, interstitial patterns on high resolution computed tomography (HRCT), and abnormal pulmonary function tests (PFTs) The aim of this study is to investigate is there any correlation between changes seen in the lung parenchyma by HRCT and the pulmonary functions of the patients.
Read the full description
This study will utilize a cross-sectional prospective study design in a single institution to investigate the correlation between CT chest findings including lung densitometry and pulmonary function test results in patients with ILD.
The study population will consist of consecutive patients diagnosed with ILD recruited from the pulmonary clinic or inpatient service.
High resolution CT chest and pulmonary function tests are routine diagnostic tests used for diagnosis of interstitial lung disease .
both tests are non invasive for the patient and will be acquired for all patients and then their results will be correlated.
Who may be able to participate?
The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.
Inclusion Criteria:
- Diagnosis of ILD (based on clinical, radiological, and pulmonary function criteria +/- histopathological criteria).
- Availability of CT chest DICOM images and pulmonary function test results (within a 2-weeks period from each other).
Exclusion Criteria:
- Pregnancy
- Pulmonary edema.
- Primary pulmonary hypertension;
- Chronic obstructive pulmonary disease
- Congestive heart failure
Study population
The study population will consist of consecutive patients diagnosed with ILD recruited from the pulmonary clinic or inpatient service. The diagnosis of ILD will be based on American Thoracic Society/European Respiratory Society (ATS/ERS) classification system for ILD.
Understand screeningTreatment, groups and participation
The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.
- Assignment
- Not reported
- Masking
- Not reported
High resolution CT Chest DIAGNOSTIC_TEST
CT chest in our institution will be done with standard high resolution protocol . No I.V contrast will be given. Scans will be obtained during full inspiration in supine position from the thoracic inlet to the level of the diaphragm.
Patients with CT chest performed outside our institution will be reviewed in DICOM format and assessed for its compatibility to be integrated into the computer-based analysis software.
Spirometry DIAGNOSTIC_TEST
Spirometry will be performed using standard techniques according to ATS-ERS criteria 2019 . Spirometry device (Zan 300, NSPIRE HEALTH GMBH Co.) will be used. Percentage predicted values (%pred) will be calculated based on reference values for healthy adults. All patients will be required to undergo spirometry in a reproducible way, and the best values will be reported. Spirometry should meet international acceptability and repeatability standards
What researchers are measuring
Outcome measures describe what is being studied. They are not proof that a treatment works.
Primary measures
CT visual Warrick score (measured by points)
Time frame: baseline
Warrick score is calculated as follow : A point value will be given to each abnormality i.e ground-glass appearance (areas of hazy opacity in the lung that do not obscure the underlying bronchial structures) = 1, irregular pleural margins = 2, septal/subpleural lines = 3, honeycombing (usually 3-10 mm in diameter and have thick walls) = 4, and subpleural cysts = 5. In each patient, the "severity of disease" score will be obtained by adding single point values (maximal severity score 15).
An "extent of disease" score is obtained by counting the number of bronchopulmonary segments involved for each abnormality as follows ; one to three segments scored as 1, four to nine segments scored as 2, and more than nine segments scored as 3 (maximal extent score 15).
The severity and extent of disease will be then calculated as the total Warrick score (range from 0 to 30)
Total lung volume, Volume of lung occupied by low attenuation areas, Volume of lung occupied by high attenuation areas, Volume of normal lung areas and volume of consolidation areas
Time frame: baseline
Total lung volume , volume of the lung occupied by low attenuation areas (attenuation values from -1024 to -950 HU; representing emphysema), volume of normally attenuated lung (from -949 to -700 HU; corresponds to healthy lung tissue) and volume of the lung occupied by high attenuation areas (between - 699 and - 250 HU) ; it represents the lung parts which are more dense than healthy lung); volume of lung with density from -249 to +40 HU, this group corresponds to areas with further increase in density, including the semi-consolidation and consolidation.
Percentage of the lung occupied by low attenuation areas, percentage of normal lung, percentage of the lung occupied by high attenuation areas and percentage of consolidation areas.
Time frame: baseline
Percentage of the lung occupied by low attenuation areas (attenuation values from -1024 to -950 HU), percentage of normal lung (from -949 to -700 HU), percentage of the lung occupied by high attenuation areas (between - 699 and - 250 HU) and percentage of consolidation areas (from -249 to +40 HU) in each lung and in each lobe.
Mean lung density of each lung, both lungs and every lobe in Hounsfield unit (HU)
Time frame: baseline
Mean lung density of each lung , both lungs and each lung lobe (e.g., upper, middle, and lower lobes) will be measured in Hounsfield unit (HU).
Forced vital capacity (FVC)
Time frame: baseline
Forced vital capacity (FVC) will be measures using spirometer and expressed as percentage.
Forced expiratory volume in 1 second (FEV1)
Time frame: baseline
Forced expiratory volume in 1 second (FEV1)
FEV1/FVC ratio
Time frame: baseline
FEV1/FVC ratio will be measures
O2 saturation
Time frame: baseline
O2 saturation is measured in percentage (SpO2) using pulse oximeter
Review the complete result tables and limitations in the official record.
Open official results ↗Research locations (1)
The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.
1 locations
Assiut University HospitalAsyut, Asyut Governorate, EgyptStatus unknown
Study team and timeline
- Lead sponsor
- Assiut University
- Study start
- Dec 1, 2026 Estimated
- Primary completion
- Dec 1, 2027 Estimated
- Study completion
- Dec 30, 2027 Estimated
- First posted
- Jul 17, 2023 Actual
- Last updated
- Nov 10, 2026 Actual
Official study contacts
Official study title
CT Quantitative Assessment of Interstitial Lung Disease Using Visual Score and Lung Densitometry Methods and Its Correlation With Pulmonary Function Tests
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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.
Retrieved: Nov 11, 2026 · Last registry update: Nov 10, 2026
