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Comparison of pharmacokinetics between continuous and intermittent vancomycin infusion

Comparison of pharmacokinetics between continuous and intermittent vancomycin infusion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092167
Enrollment
Unknown
Registered
2024-11-12
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Infection

Interventions

Loading group:The first dose was given a loading dose (1.5 times the maintenance dose), followed by a regular dose of 15mg/Kg q8h or q12h or q24h, the specific frequency adjusted according to creatini
Continuous infusion group:The initial dose of 20mg/Kg was given continuously after surgery, followed by a maintenance infusion of 15-40mg/Kg, depending on creatinine clearance, for 14 days.

Sponsors

Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Hospitalization at the Research Center Hospital from January 1, 2025 to December 31, 2027 2. Use vancomycin for empirical or targeted treatment 3. Age =18 years old 4. Voluntarily (or legal agent agrees) to participate in the study and sign the informed consent

Exclusion criteria

Exclusion criteria: 1. Vancomycin was used within 3 days before enrollment 2. Pregnancy or breastfeeding 3. Patients with deteriorating renal function: patients with creatinine rising =10µmol/L per day 4. Clinical investigator participating in another investigational drug or investigational device within 3 months prior to the trial; 5. The subject is unable or unwilling to comply with study specific procedures and restrictions; 6. The investigator judged that he could not complete the study or it was not appropriate to participate in the study (expected to die within 72 hours, the patient refused active treatment).

Design outcomes

Primary

MeasureTime frame
Concentration of Vancomycin;

Secondary

MeasureTime frame
Creatinine;

Countries

China

Contacts

Public ContactHuang Yanxia

Ruijin Hospital

513273126hyx@sina.com+86 182 1754 9397

Outcome results

None listed

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