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A Multicenter Randomized Controlled Clinical Study of Xiaoer Feire Kechuan Granule in the Treatment of Children's influenza (Syndrome of Heat Toxicity Attacking the Lung)

A Multicenter Randomized Controlled Clinical Study of Xiaoer Feire Kechuan Granule in the Treatment of Children's influenza (Syndrome of Heat Toxicity Attacking the Lung)

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076111
Enrollment
Unknown
Registered
2023-09-25
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-10-03

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

Conditions

influenza

Interventions

Test group:Xiao'er Feire Kechuan Granules

Sponsors

Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 14 Years

Inclusion criteria

Inclusion criteria: Only those who meet all the following criteria can be selected (1) Comply with the clinical diagnosis of influenza in the influenza diagnosis and treatment plan (2020 version) in 2020; (2) Those who comply with traditional Chinese medicine syndrome differentiation and are classified as heat toxin attacking lung syndrome; (3) Age 1-14 years old; (4) Disease duration = 72 hours; (5) Agree to cooperate with medication and undergo evaluation according to the requirements of the experimental protocol; (6) Must obtain the informed consent of the legal guardian of the subject and voluntarily sign the informed consent form; When the subject is able to make a decision to participate in a clinical trial, they must also obtain their own consent.

Exclusion criteria

Exclusion criteria: Those who meet any of the following criteria need to be excluded (1) Have used drugs that may affect the evaluation of the trial efficacy within the past week (such as antipyretic and analgesic drugs, antibiotics, H1 receptor blockers, vasoconstrictors, etc.); (2) Patients treated with systemic steroid or other immunosuppressive agents; (3) Individuals with a history of liver disease; (4) Those who have already discovered shadows or signs of infection in the lungs; (5) Individuals with severe liver, kidney, heart, vascular, neurological, endocrine, immune function disorders, or cancer; (6) Those who are clearly allergic to the experimental drug or its formulation components, or have allergic constitution; (7) Those who have participated in clinical trials within 3 months; (8) White blood cell count is too high (>50 * 109/L) or too low (<4 * 109/L); (9) Researchers believe that individuals should not be included.

Design outcomes

Primary

MeasureTime frame
Clinical total effective rate;Changes in main symptom scores;

Secondary

MeasureTime frame
Secondary symptom score changes;Changes in tongue pulse integral;Usage of symptomatic treatment drugs;

Countries

China

Contacts

Public ContactXuefeng Wang

Affiliated Hospital of Liaoning University of Traditional Chinese Medicine

lnzywxf@163.com+86 138 4020 8807

Outcome results

None listed

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