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An Observational, Prospective, Multicenter Study to Evaluate the Biologic Use and Outcomes in Chinese Asthma Patients
An Observational, Prospective, Multicenter Study to Evaluate the Biologic Use and Outcomes in Chinese Asthma Patients
Active Not RecruitingN/A
Sponsor: AstraZeneca
Conditions: Asthma
Countries: China
This study is a multicenter, observational, prospective study to evaluate the asthma biologic use features and clinical outcomes in China. Patients will undergo clinical assessments and receive standard medical care as determined by the treating physician.
Eligibility overview
Sex: ALL
Healthy volunteers: Yes
Study type: OBSERVATIONAL
Eligibility criteria
Inclusion Criteria: 1. Chinese, Female or Male 2. Age: no limitation 3. Physician-confirmed asthma diagnosis with documented evidence of diagnosis or evidence of variable expiratory airflow limitation (e.g., from bronchodilator reversibility testing or other tests). 4. Participants or their legal guardians must be able to provide informed consent. 5. Prescription of asthma biologics at enrolment. Exclusion Criteria: 6. Participation in an interventional study within the last 3 months. 7. Any significant disease or disorder which, in the opinion of the investigator, may either put the patient at risk because of participation in the study with the usage of biologics, or may influence the results of the study, or the patient's ability to participate in the study
Locations (30)
- Hohhot, China, China
- Beijing, China
- Changsha, China
- Chengdu, China
- Foshan, China
- Fuzhou, China
- Guangzhou, China
- Hangzhou, China
- Hefei, China
- Jinan, China
- Kunming, China
- Nanchang, China
- Nanjing, China
- Ningbo, China
- Qingdao, China
- Quanzhou, China
- Shanghai, China
- Shenyang, China
- Shenzhen, China
- Shijiazhuang, China
- Suining, China
- Taiyuan, China
- Tianjin, China
- Ürümqi, China
- Wenzhou, China
- Wuhan, China
- Wuxi, China
- Xi'an, China
- Zhengzhou, China
- Zhuhai, China