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The value of YKL-40 in the evaluation of asthma condition and curative effect

The value of YKL-40 in the evaluation of asthma condition and curative effect

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036524
Enrollment
Unknown
Registered
2020-08-24
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-14

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

Conditions

asthma

Interventions

case series:Nil

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) The subjects volunteered to participate in the study and strictly abide by the research regulations, understand and comply with the corresponding inspection, comply with the dosage and follow-up plan, and voluntarily sign the written informed consent; 2) They are 14-80 years old, regardless of gender and race; 3) Wheezing, shortness of breath, chest tightness or cough recurrently; 4) Wheezing was heard in both lungs; 5) The above symptoms can be relieved by themselves or after treatment; 6) Except wheezing, shortness of breath, chest tightness or cough caused by other diseases; 7) Patients with atypical symptoms should have at least one of the following tests positive: (1) Bronchial provocation test was positive; (2) FEV1 increased by more than 12% and the absolute value of FEV1 increase was more than 200 ml; (3) The diurnal variation rate of peak expiratory flow (PEF) within one week was more than 10%. Those who meet the above 7 items will be selected.

Exclusion criteria

Exclusion criteria: 1) Those who cannot cooperate with related inspections of this project or cannot cooperate for other reasons; 2) With COPD, interstitial pneumonia, active tuberculosis, community-acquired pneumonia, lung cancer, bronchiectasis, pulmonary heart disease, pulmonary embolism; combined with diseases of other systems (coronary heart disease, myocarditis, heart failure, GERD, neuromuscular disease); 3) Alcohol or narcotic drug abuse, history of drug abuse, or history of mental illness (such as schizophrenia, obsessive-compulsive disorder, depression), confrontational personality, bad motivation, suspiciousness or other emotional or intellectual problems, etc. may affect the effectiveness of the informed participation in this study Sexual situation; 4) Participating in other drug clinical trials, or stopping for less than 3 months; 5) Those with pregnancy; 6) Patients with obvious abnormalities in chest HRCT.

Design outcomes

Primary

MeasureTime frame
YKL-40;

Countries

China

Contacts

Public ContactBenSuqin

Shanghai General Hospital

bensuqin@163.com+86 13681731135

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026