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A Single-blind, Double-arm, Randomized Controlled Study of the Efficacy and Safety of Pediatric Dingchuan Oral Solution in the Treatment of Acute Attacks of Bronchial Asthma in Children (Febrile Asthma Syndrome)

A Single-blind, Double-arm, Randomized Controlled Study of the Efficacy and Safety of Pediatric Dingchuan Oral Solution in the Treatment of Acute Attacks of Bronchial Asthma in Children (Febrile Asthma Syndrome)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105482
Enrollment
Unknown
Registered
2025-07-04
Start date
2025-07-07
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Asthma

Interventions

Control group:Conventional drug therapy
Treatment group:Pediatric asthma oral solution Conventional drug therapy

Sponsors

the Children’s Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria defined in GINA (2025) and the Guidelines for the Diagnosis and Prevention of Bronchial Asthma in Children; 2. Meet the TCM syndrome differentiation criteria for febrile asthma syndrome; 3. Those with asthma exacerbation severity graded as mild; 4. Age 6~13 years old (= 8 years old) jointly signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Children with bronchial asthma in the critical stage, or those with fever within <=48h at the time of screening, as well as complicated by laryngitis, pneumonia, sepsis and other diseases; 2. Children with other diseases that can cause asthma or dyspnea, children with tuberculosis, pulmonary interstitial fibrosis, bronchiectasis, thoracic deformity and other diseases; 3. Children with severe malnutrition, rickets and serious primary diseases such as heart, brain, liver, kidney, hematopoietic system, psychiatry, and nervous system; 4. Those who had respiratory tract infection within 6 weeks before selection; 5. Those whose asthma exacerbation severity is graded as severe; 6. Those who are allergic to the test drug or have relevant drug contraindications; 7. Children who participated in other clinical trials within 1 month; 8. Those who are considered by the investigator to be inappropriate to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Clinical improvement rate;

Countries

China

Contacts

Public ContactLanfang Tang

the Children’s Hospital of Zhejiang University School of Medicine

6195007@zju.edu.cn+86 138 6813 8022

Outcome results

None listed

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