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Randomized, parallel-controlled clinical observation of the efficacy and safety of Qingxuan cough granules in the treatment of pediatric acute bronchitis (wind fever offender lung evidence)

Randomized, parallel-controlled clinical observation of the efficacy and safety of Qingxuan cough granules in the treatment of pediatric acute bronchitis (wind fever offender lung evidence)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072051
Enrollment
Unknown
Registered
2023-06-01
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Acute bronchitis in children

Interventions

Experimental group:Qingxuan cough granules
Control group:Pediatric pulmonary fever cough and asthma granules

Sponsors

The First Affiliated Hospital of Henan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 14 Years

Inclusion criteria

Inclusion criteria: (1) Meet the diagnostic standards of western medicine for pediatric acute bronchitis; (2) Age 4~14 years old (including boundary value), gender is not limited; (3) daytime cough symptom score = 4 or nighttime cough symptom score =4 points; (4) Within 72 hours after the onset of acute bronchitis, no drugs with cough and phlegm effect have been used before the visit; (5) The legal guardian of the child agrees that the child will participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Children with a maximum body temperature of > 38.5°C within 24 hours before enrollment; (2) Children with acute infectious diseases such as measles, pertussis, influenza, etc.; (3) Children with acute upper respiratory tract infection, bronchial asthma, bronchiolitis, wheezing bronchitis, bronchial pneumonia and other respiratory diseases; (4) Children with allergies to the study drug or its components; (5) Children with malnutrition, immune deficiency and tuberculosis; (6) Children who have participated in or are participating in clinical observation of other drugs within 1 month; (7) Children with severe primary diseases such as heart, liver, kidney, digestive and hematopoietic systems; (8) Children judged by the investigator to be unsuitable for clinical observation.

Design outcomes

Primary

MeasureTime frame
Clinical healing rate and effective rate of cough;

Countries

China

Contacts

Public ContactYan Yong Bin

The First Affiliated Hospital of Henan University of Chinese Medicine

15515730918@163.com+86 155 1573 0918

Outcome results

None listed

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