Antibiotics Clinical Trial
Official title:
A Prospective,Multicenter,Non-interventional Real-world Study for Standardized Clinical Application of Antibacterial/Anitifungal Drugs
The purpose of this real world study is to observe the clinical status for standardized using of antibacterial/anitifungal drugs in patients with infection,and to evaluate the efficacy and safety of anti-infection therapy.
Status | Not yet recruiting |
Enrollment | 5000 |
Est. completion date | December 31, 2022 |
Est. primary completion date | June 30, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Hospitalized patients (= 18 years old) -= 3 days receiving antibacterial/antifungal drugs therapy Exclusion Criteria: - |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Peking University People's Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of standardized using of antibacterial/antifungal drugs | the proportion of cases who receive standardized antibacterial/antifungal drugs therapy | approximately 6 months after completion of data collection | |
Primary | Clinical efficacy rate | the clinical efficacy evaluation of antibacterial/antifungal drugs therapy | approximately 6 months after completion of data collection | |
Secondary | Microbiological efficacy rate | the microbiological efficacy evaluation of antibacterial/antifungal drugs therapy | approximately 6 months after completion of data collection | |
Secondary | Overall efficacy rate | the overall efficacy evaluation of antibacterial/antifungal drugs therapy based on clinical and microbiological efficacy outcome | approximately 6 months after completion of data collection | |
Secondary | All-cause mortality | the evaluation of all-cause mortality | approximately 6 months after completion of data collection | |
Secondary | Antibacterial/antifungal drugs-Related Adverse Events | only evaluate of the adverse events related to antibacterial/antifungal drugs | approximately 6 months after completion of data collection |
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