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Registry Study on the Utilization Status of Compound Cold Medicines in Pediatrics

Registry Study on the Utilization Status of Compound Cold Medicines in Pediatrics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110734
Enrollment
Unknown
Registered
2025-10-20
Start date
2025-10-23
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Upper respiratory tract infections and influenza

Interventions

Observer group (Compound Paracetamol and Methylephedrine Oral Solution):None
Control group (Pediatric Paracetamol, Atificial Cow-bezoar and Chlorphenamine Maleate Granules):None
Control group (Compound Paracetamol and Dextromethorphan Syrup):None
Control group (Paracetamol,Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide for Suspension):None

Sponsors

Jiangxi Provincial Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 15 Years

Inclusion criteria

Inclusion criteria: 1.The clinical diagnosis is upper respiratory tract infection or influenza; 2.The prescription contains Compound Paracetamol and Methylephedrine Oral Solution or Pediatric Paracetamol, Atificial Cowbezoar and Chlorphenamine Maleate Granules or Paracetamol,Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide or Compound Paracetamol and Dextromethorphan Syrup; 3 months <= age <= 15 years old; 3.The legal guardian signs the informed consent form, and patients aged 8 years and above also sign the informed consent form themselves.

Exclusion criteria

Exclusion criteria: 1.Based on the researchers' assessment, they determined that the individuals were not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
The disappearance time of single symptoms such as nasal congestion and runny nose, cough, and fever.;The score of the Clinical Global Impression Improvement Scale - Improvement (CGI-I) at the end of taking the medicine.;The changes in the functional dimension and the dimension affecting parents from the baseline on the 1st, 2nd, 3rd, 5th, and 7th after taking the medicine.;The changes in the symptom dimension scores of the Chinese version of the "Canadian Acute Respiratory Disease and Influenza Scale" on the 2nd and 3rd days of medication compared with the baseline.;Recovery rate of upper respiratory tract infection on the 3rd, 5th, and 7th days after taking the medicine;Relief rate of influenza on the 3rd, 5th and 7th days after taking medicine.;Relief time of influenza;On days 2 and 3 of medication, symptom dimension scores of the Chinese version of the "Canadian Acute Respiratory Disease and Influenza Scale" decreased by =50% from baseline.;Recovery time of upper respiratory tract infection;Complete fever reduction time;The disappearance rate of single symptoms such as nasal congestion and runny nose, cough and fever on the 2nd and 3rd days of taking the medicine.;

Secondary

MeasureTime frame
Types and incidence rates of adverse reactions;

Countries

China

Contacts

Public ContactChen Qiang

Jiangxi Provincial Children's Hospital

jx-cq@163.com+86 13907099745

Outcome results

None listed

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