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Evaluation of the efficacy and safety of five generations of cephalosporins in the treatment of Staphylococcus aureus bacteremia

Evaluation of the efficacy and safety of five generations of cephalosporins in the treatment of Staphylococcus aureus bacteremia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099508
Enrollment
Unknown
Registered
2025-03-25
Start date
2024-02-26
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Staphylococcemia

Interventions

Research group:Cefbiroxime sodium for Injection, Specification: 500 mg, Manufacturer: Nipro Pharma Corporation-Odate Plant. 500mg was intravenously infused every 2 hours every 8 hours, and the investi

Sponsors

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine (SRRSH)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Subjects must meet all of the following enrollment criteria to enter this trial. 1. Age >= 18 years; 2. Meet clinical and laboratory diagnostic criteria for Staphylococcus aureus bacteremia (SAB) or methicillin-resistant Staphylococcus aureus (MRSA) infection; 3. Voluntary participation in this study and signed informed consent. If the subject is unable to read the informed consent form (e.g. illiterate subject), witnesses are required to witness the informed process and sign informed consent.

Exclusion criteria

Exclusion criteria: Subjects shall be excluded from this study if they meet any of the following criteria. 1. Definite bloodstream or non-bloodstream concomitant infection with a gram-negative resistant organism that is not susceptible to the test drug; 2. Patients with SAB who have been treated with potentially effective (anti-staphylococcal) systemic antimicrobial therapy for more than 48 h (with the exception of poor efficacy) in the 7 days prior to enrollment, with the exception of clearly documented bloodstream clearance failures; 3. Vulnerable groups, including those with mental illness, cognitive impairment, critically ill patients, and pregnant women. 4. Those deemed unsuitable for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
Clinical cure rate (7-14 days after last treatment or before discharge);Microbial eradication rate (HAP CAP or SAB 7-14 or 70 days after the last treatment, and before discharge, respectively);Early clinical response (3 or 4 days after first treatment);Clinical failure rate (7-14 days after last treatment or before discharge);

Countries

China

Contacts

Public ContactYu Yunsong/Du Xiaoxing

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine (SRRSH)

duxiaoxing2000@163.com+86 136 6669 7278

Outcome results

None listed

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