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A superiority designed study of Uygur medicine Luo-Ou-Ke Zu-Pa and Chinese medicine Xiao-Qing-Long-Tang Decoction in the treatment of cold asthma

A superiority designed study of Uygur medicine Luo-Ou-Ke Zu-Pa and Chinese medicine Xiao-Qing-Long-Tang Decoction in the treatment of cold asthma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035579
Enrollment
Unknown
Registered
2020-08-14
Start date
2021-03-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

asthma

Interventions

Sponsors

Huashan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years old at the time of enrollment; 2. Patients with bronchial asthma diagnosed by modern medicine, regular inhaled hormone therapy or other conventional treatment 3 months later, patients with bronchial asthma ACT score <20 points; 3. Patients with abnormal mucus type identified by Uighur medicine; 4. Patients without upper and lower respiratory tract infections and not taking oral and intravenous glucocorticoid therapy within 2 weeks; 5. Subjects voluntarily participated in the study and signed Informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients in acute attack stage, who need oral and intravenous glucocorticoid therapy; 2. Patients with abnormal blood type, abnormal savda type, and abnormal biliary type identified by Uygur medicine; 3. Combined Patients with COPD, pulmonary fibrosis, and a history of lung resection; 4. Pregnant or planning to become pregnant or breastfeeding women; 5. Patients with malignant tumors and hematological diseases; 6. Those who have participated in clinical trials of other drugs within 3 months; 7. Those with severe impairment of heart, liver, and kidney functions (heart function grades 3 to 4, ALT and/or AST exceeding 1.5 times the upper limit of normal, and Cr exceeding the upper limit of normal); 8. Those deemed unsuitable for inclusion by the investigator Other situations.

Design outcomes

Primary

MeasureTime frame
ACT;Peak expiratory flow rate (PEF) value and average daily diurnal variation rate;Exhaled nitric oxide (FeNO);

Countries

China

Contacts

Public ContactJingcheng Dong

Huashan Hospital Affiliated to Fudan University

JCdong2004@126.com+86 13601761761

Outcome results

None listed

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