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Retrospective study on the clinical efficacy of Qingjin Xiaoyan Decoction in the treatment of community-acquired pneumonia

Research on the Academic Thought and Clinical Experience Inheritance of Professor Gao Feng

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082169
Enrollment
Unknown
Registered
2024-03-22
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Community acquired pneumonia

Interventions

Oral Qingjin Xiaoyan Decoction for 5 days:None
Oral Qingjin Xiaoyan Decoction for 7 days:None
Oral Qingjin Xiaoyan Decoction for 10 days:None
Oral Qingjin Xiaoyan Decoction for 12 days:None
Oral Qingjin Xiaoyan Decoction for 14 days:None

Sponsors

Wangjing Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Meets the diagnostic criteria for community-acquired pneumonia; ? Meets the diagnostic criteria for phlegm heat obstructing lung syndrome in wind warm lung heat disease; ? Age range from 18 to 75 years old; ? Regular oral administration of Qingjin Xiaoyan Decoction for more than 5 days.

Exclusion criteria

Exclusion criteria: ? Patients with severe chronic diseases such as malignant tumors, severe liver and kidney dysfunction, and severe cardiovascular and cerebrovascular diseases; ? Irregular medication users; ? Cases where the description of case data is not standardized and symptoms cannot be quantified through symptom integration even after data normalization.

Design outcomes

Primary

MeasureTime frame
Overall efficacy;

Secondary

MeasureTime frame
Record antibiotic treatment course;Antipyretic time;Traditional Chinese Medicine Symptom Score;

Countries

China

Contacts

Public ContactLiu Huimei

Wangjing Hospital, China Academy of Chinese Medical Sciences

liuhuimei2008@126.com+86 138 1197 9733

Outcome results

None listed

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