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A medical records based study for Keganliyan oral liquid in the treatment of children with upper respiratory system diseases

Keganliyan oral liquid for children with upper respiratory system diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200063328
Enrollment
Unknown
Registered
2022-09-04
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

children with upper respiratory system diseases

Interventions

case series:case series

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 14 Years

Inclusion criteria

Inclusion criteria: 1. From May 31, 2016 to May 31, 2022 at the target center: outpatient or inpatient cases with Keganliyan oral liquid prescribed; 2. TCM hospitals meet the diagnostic criteria of TCM wind-heat and cold syndrome (not required by western medicine hospitals); 3. Meet the diagnostic criteria of Western medicine for acute upper respiratory tract infection accompanied by pharyngeal swelling and pain; 4. Children aged 3 to 14 years old, regardless of gender.

Exclusion criteria

Exclusion criteria: 1. Cases are combined use of other Chinese patent medicines for the treatment of wind-heat and cold syndrome.

Design outcomes

Primary

MeasureTime frame
Distribution of patients' drug use and diseases (department, disease diagnosis);Observation of the characteristics of the drug population (demographic characteristics);Clinical application characteristics of Keganliyan oral liquid (dosage, frequency, cycle, combined treatment plan);Adverse events/adverse reactions;Subgroup stratified analysis (record analysis if available, not if not);

Countries

China

Contacts

Public ContactTeng Huang
dapengnanfei@163.com+86 13538971638

Outcome results

None listed

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