Efficacy and Safety of Intramuscular Injection of Xiyanping Injection in the Treatment of Acute Bronchitis in Children

Sponsor
Jiangxi Qingfeng Pharmaceutical Co. Ltd. (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT04926506
Collaborator
(none)
80
2
14.7

Study Details

Study Description

Brief Summary

Any pathogen that causes an upper respiratory tract infection can cause bronchitis.The primary pathogen is virus. On the basis of virus infection, pathogenic bacteria may cause secondary infection or co-infection。Xiyanping injection is mainly used in the treatment of bronchitis by intravenous injection。

Condition or Disease Intervention/Treatment Phase
  • Drug: Xiyanping injection
N/A

Detailed Description

To further verify the clinical value and safety of intramuscular injection of Xiyanping injection in the treatment of acute bronchitis in children, provide reference for subsequent validation studies, and provide more reasonable and standard application guidance and basis for clinical practice.A multicenter, randomized, parallel controlled study was conducted on the treatment of acute bronchitis by intramuscular injection of Xiyanping injection.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy and Safety of Intramuscular Injection of Xiyanping Injection in the Treatment of Acute Bronchitis in Children: a Multicenter, Randomized, Parallel Controlled Clinical Study
Anticipated Study Start Date :
Oct 8, 2021
Anticipated Primary Completion Date :
Sep 21, 2022
Anticipated Study Completion Date :
Dec 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Xiyanping injection combined with routine treatment

Drug: Xiyanping injection
Intramuscular injection of Xiyanping injection, 0.3mL / (kg.d) daily, Bid

No Intervention: routine treatment

Outcome Measures

Primary Outcome Measures

  1. Total clinical effective rate [up to day 7]

    The children were evaluated according to the improvement of body temperature (axillary temperature), cough, expectoration, lung rales and other symptoms and signs and the improvement time

Secondary Outcome Measures

  1. Cough easing [up to day 7]

    Symptoms are less than or equal to 1 point (mild) and remain for 24 hours or more

  2. Lung rales relieved [up to day 7]

    Symptoms are less than or equal to 1 point (mild) and remain for 24 hours or more

  3. Fever relief [up to day 7]

    Body temperature <37.5℃ (axillary temperature) and maintained for 24h or more

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year to 6 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age: 1-6 years (>1 years, ≤6years);

  2. Children who meet the diagnosis criteria of acute bronchitis in children;

  3. All symptoms, including cough, had been present for less than 72 hours at the time of inclusion screening;

  4. The informed consent process complies with the regulations, and the legal guardian signs the informed consent.

Exclusion Criteria:
  1. Have used Chinese medicine injection containing andrographolide and similar functions (clearing heat and detoxifying, relieving cough and stopping dysentery) or oral dosage within 72 hours.

  2. Children with severe bronchitis or early pneumonia;

  3. Children with acute infectious diseases such as measles, pertussis,influenza and hand-foot-and-mouth disease;

  4. Children with diseases such as acute upper respiratory tract infection, suppurative tonsillitis, wheezing bronchitis, bronchial asthma, bronchiolitis pneumonia, tuberculosis, tumor;

  5. neutrophil granulocyte>80%, or those who need antibiotic therapy;

  6. Children with severe malnutrition and immunodeficiency;

  7. Children with severe primary diseases such as heart, liver, kidney, digestion and hematopoietic system;

  8. Allergic constitution and children allergic to the drug used in this study;

  9. Children who are taking epinephrine, isoproterenol and other catecholamines;

  10. Children who are taking MAO inhibitors or tricyclic antidepressants

  11. Children who are taking non-selective β-blockers such as Propranolol;

  12. Those who are not included based on the investigators judgment.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Jiangxi Qingfeng Pharmaceutical Co. Ltd.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jiangxi Qingfeng Pharmaceutical Co. Ltd.
ClinicalTrials.gov Identifier:
NCT04926506
Other Study ID Numbers:
  • QF-XYP2021-1
First Posted:
Jun 15, 2021
Last Update Posted:
Oct 4, 2021
Last Verified:
Jun 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 4, 2021