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The Registration on the Use of Feilike Heji in Minors

A Study on the Registration of the Use of Feilike Heji in Minors

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04658992
Enrollment
3000
Registered
2020-12-09
Start date
2020-12-15
Completion date
2022-03-01
Last updated
2021-08-04

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

Conditions

Bronchial Asthma

Brief summary

Feilike HeJi is produced by Guizhou Jianxing Pharmaceutical Co. LTD. For the treatment of phlegm heat caused by lung cough phlegm yellow, bronchial asthma, bronchitis, see the syndrome of proprietary Chinese medicine (approval number: Z20025136) approved by the state and the drug from radix scutellariae, radix peucedani, radix stemonae, red gentian root of deal, phoenix tree, spreading hedyotis herb, red tube 7 flavour, with qingrejiedu, antitussive expectorant effect. In order to fully understand the safety of Feilike HeJi in clinical practice and fulfill the responsibility of production enterprises for patients, the production enterprises initiated this study to further evaluate the safety and understanding of the function characteristics of Feilike HeJi in a wide range of people, so as to guide the clinical rational drug use.

Interventions

None listed

Sponsors

China Academy of Chinese Medical Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

* All minor patients (age \<18 years old) who use Feilike Mixture at the specified monitoring time and in the monitoring center (department) . * Voluntarily participate in this study and meet ethical requirements.

Exclusion criteria

* Not Applicable.

Design outcomes

Primary

MeasureTime frameDescription
AEThe range of adverse events was from the beginning of the use of Feilike HeJi to 3 days after the cessation of the use of Feilike HeJi.All adverse events occurred during the study were determined according to CTCAE V5.0 for severity.

Countries

China

Contacts

Primary ContactJing Liu, Prof
lljjred@126.com010-59616885

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026