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Study on the mechanism of Tanreqing injection combined with antibiotics on respiratory system-related drug-resistant bacteria based on drug resistance sensitization

Study on the mechanism of Tanreqing injection combined with antibiotics on respiratory system-related drug-resistant bacteria based on drug resistance sensitization

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2022000021
Enrollment
Unknown
Registered
2022-06-17
Start date
2022-06-22
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

bacterial infection

Interventions

control group:Ceftazidime for Injection
Trial group:Ceftazidime for Injection + Tanreqing Injection

Sponsors

Medical Experimental Center of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Meet the diagnostic criteria of lower respiratory tract infection (pneumonia, acute exacerbation of chronic obstructive pulmonary disease, bronchiectasis complicated infection) and need antibiotic treatment; ?Age between 40 and 80 years old (including 40 and 80 years old); ? Obtain qualified sputum specimens of the lower respiratory tract (sputum smear: =10 squamous epithelial cells in each low-power microscope field, and =25 leukocytes per low-power field), and the sputum bacteria were cultured as drug-resistant Pseudomonas aeruginosa bacteria; ? In line with the syndrome of phlegm-heat obstructing the lung; ? Accept the treatment plan voluntarily and sign the informed consent.

Exclusion criteria

Exclusion criteria: ? Pulmonary tuberculosis patients; ? Non-resistant Pseudomonas aeruginosa infection; ? Immunodeficiency patients or taking immunosuppressive agents or glucocorticoids within the past 3 months; ? Patients with severe liver and kidney dysfunction, severe pulmonary heart disease with heart failure or hematopoietic system and other serious primary diseases; ? Pregnant and lactating patients; ? Those who are allergic to the study drug or its components; ? Other doctors think that it is not suitable to participate in this researcher.

Design outcomes

Primary

MeasureTime frame
Drug allergy testing;

Secondary

MeasureTime frame
16S rDNA, metagenomic sequencing;

Countries

China

Contacts

Public ContactWang Yi

Medical Experimental Center of China Academy of Chinese Medical Sciences

Prof.wangyi@foxmail.com13552445935

Outcome results

None listed

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