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Public Title:A Study on the Registration of The Use of Feilike HeJi in Adults

Scientific Title:A Study on the Registration of The Use of Feilike HeJi in Adults

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04714489
Enrollment
3000
Registered
2021-01-19
Start date
2021-01-16
Completion date
2021-08-01
Last updated
2021-06-28

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

OTHERNO.

NO.

Sponsors

China Academy of Chinese Medical Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* All adult patients (age ≥18 years old) who use Feilike HeJi at the specified monitoring time and in the monitoring center (department) ; * Must voluntarily participate in this study; * Must meet ethical requirements.

Exclusion criteria

* NO

Design outcomes

Primary

MeasureTime frameDescription
AEFrom the prescription of Feilike HeJi to 3 days after stop using Feilike HeJi.All the data to be collected are included in Table A and Table B of the registration And Research Information collection of Adults using Feilike HeJi.Data in Table A are filled in by authorized researchers (such as clinicians) and patients, and data in Table B are filled in by authorized researchers (such as clinicians).

Countries

China

Contacts

Primary ContactHongchun Zhang, M.D.
13701226664@139.com+86 13701226664

Outcome results

None listed

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