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A study to evaluate the efficacy and safety of CHL-025 intake for improving respiratory health.

A 12-week, multicenter, randomized, double-blind, placebo-controlled clinical trial to evaluate efficacy and safety for improvement of CHL-025 on respiratory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0012058
Enrollment
100
Registered
2026-05-28
Start date
2025-01-10
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Dietary Supplement : Test food: Oral administration of 2 tablets once daily for 12 weeks, containing CHL-025 as the main ingredient. Control food: Oral administration of 2 tablets once daily for 12 we

Sponsors

CHLabs
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult men and women aged 19 to 80 years at the time of screening 2) Individuals who have experienced persistent symptoms of respiratory discomfort (cough, phlegm, shortness of breath, or chest tightness, etc.) for at least one month prior to the screening test 3) Individuals who voluntarily consent to participate in this human clinical trial and possess the ability to understand and comply with the trial methods and procedures

Exclusion criteria

Exclusion criteria: 1) Current smokers or those who have started quitting smoking within the last 3 months 2) Individuals with clinically significant findings of respiratory disease on chest X-ray (bronchiectasis, active tuberculosis, pneumonia, etc.) or those diagnosed with asthma or chronic obstructive pulmonary disease (COPD) based on pulmonary function tests (however, those who do not require regular medication are eligible for registration) 3) Individuals with clinically significant acute or chronic cardiovascular, endocrine, immune, hepatobiliary, renal and urinary, neuropsychiatric, musculoskeletal, inflammatory, hematological/neoplastic, or gastrointestinal diseases requiring treatment 4) Individuals who have taken medications or health functional foods related to respiratory health within the last 4 weeks prior to the screening test 5) Individuals who have consumed immunosuppressants or glucocorticoids within the last 3 months 6) Individuals who are drug addicts or have a history of or are suspected of drug abuse 7) Individuals who are sensitive to or have allergies/side effects to ingredients contained in the test and control foods 8) Individuals who have participated in or plan to participate in other human application trials or clinical trials within the last 3 months 9) Individuals showing results corresponding to the following in diagnostic medical tests - AST, ALT > 3 times the reference value - Serum creatinine > 2.0mg/Dl 10) Pregnant, breastfeeding, or planning to become pregnant during the study period 11) Alcoholics or excessive drinkers - Men: > 40g/day (approximately 4 glasses of beer or 4 glasses of soju) - Women: > 20g/day (approximately 2 glasses of beer or 2 glasses of soju) 12) Individuals deemed unsuitable for participation in the study by the Principal Investigator due to diagnostic medical test results or other reasons

Design outcomes

Primary

MeasureTime frame
St. George's respiratory questionnaire;Superoxide Dismutase

Secondary

MeasureTime frame
Lung function tests;Inflammatory markers;Breathlessness, Cough, and Sputum Scale;Visual Analogue Scale;modified Medical Research Council dyspnea scale;Cough Assessment Test;Leicester Cough Questionnaire

Countries

Korea, Republic of

Contacts

Public ContactYoung IL Hwang

Hallym University Medical Center

hyicyk@gmail.com+82-31-380-3175

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Jun 11, 2026