Trials / Completed
CompletedNCT00780351
Dosing Vancomycin in Patients on Sustained Low Efficiency Daily Hemodiafiltration (SLEDD-f)
Pharmacokinetics and Dosing of Vancomycin in Sustained Low Efficiency Daily Hemodiafiltration (SLEDD-f)
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 15 (estimated)
- Sponsor
- National Taiwan University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
1. Sustained low efficiency daily hemodiafiltration(SLEDD-f) is a kind of renal replacement therapy with high-flux dialyser membrane (helixone). 2. The pore size of helixone is larger than most antibiotics, and vancomycin is supposed to be removed during dialysis. 3. Our study wants to find the amount of vancomycin removed during SLEDD-f, and try to find the most appropriate dose regimen for this kind of patients.
Detailed description
Vancomycin is the most important antibiotic in the treatment of resistant G(+) bacteria infections. Close monitor of serum level is important to ensure its safety and effectiveness. So far there is not enough data to support the optimal dose regimen of vancomycin in patients on SLEDD-f. In this study, we draw blood levels between 2 doses of vancomycin to determine the pharmacokinetic parameters of vancomycin and fraction removed by SLEDD-f so as to determine the most appropriate dose regimen.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | sustained low efficiency daily hemodiafiltration (SLEDD-f) | vancomycin 15mg/kg IV infusion on day 1 from 6PM to 8PM. Start SLEDD-f on day 2 from 9AM to 5PM. |
Timeline
- Start date
- 2008-10-01
- Completion
- 2009-08-01
- First posted
- 2008-10-27
- Last updated
- 2009-10-23
Locations
1 site across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT00780351. Inclusion in this directory is not an endorsement.