None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adults aged 19 years or older Non-smokers or former smokers who have abstained from smoking for at least one year Individuals who submit the results of a health screening conducted within the past year by the National Health Insurance Service (NHIS) or an equivalent examination; if such documentation is unavailable, participants will undergo tests corresponding to NHIS health screening items to confirm the absence of any uncontrolled acute or chronic diseases
Exclusion criteria
Exclusion criteria: - Individuals with clinically significant acute or chronic diseases requiring treatment, including but not limited to cardiovascular, cerebrovascular, endocrine, immune, respiratory, hepatobiliary, renal and urinary, neuropsychiatric, musculoskeletal, inflammatory, hematologic/oncologic, or gastrointestinal disorders - Individuals with contraindications or precautions for the study drug, including known hypersensitivity to this drug or its components, patients with gastric or duodenal ulcers, galactose intolerance, or lactase deficiency - Pregnant or breastfeeding women - Individuals deemed by the investigator to be unsuitable for participation in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cytokines: IL-6, IL-8, IL-10, IL-1ß (interleukin-1 beta), TNF-a (tumor necrosis factor-alpha), IFN-? (interferon-gamma);Exhaled nitric oxide (FeNO);Blood pressure: Systolic blood pressure (SBP) and diastolic blood pressure (DBP);Pulmonary function test: FEV1 (Forced Expiratory Volume in 1 second), FVC (Forced Vital Capacity), and FEV1/FVC ratio | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart Rate | — |
Countries
Korea, Republic of
Contacts
Inha University Hospital