ClinicalTrials.Veeva

Menu

Dosing Vancomycin in Patients on Sustained Low Efficiency Daily Hemodiafiltration (SLEDD-f)

National Taiwan University logo

National Taiwan University

Status

Completed

Conditions

Acute Renal Failure

Treatments

Device: sustained low efficiency daily hemodiafiltration (SLEDD-f)

Study type

Observational

Funder types

Other

Identifiers

NCT00780351
200705036M

Details and patient eligibility

About

  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.

Full 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.

Enrollment

15 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Acute renal failure of any cause
  • Use SLEDD-f as renal replacement therapy
  • Priscribe vancomycin for a known or suspected infection

Exclusion criteria

  • None

Trial design

15 participants in 1 patient group

SLEDD-f, vanco
Description:
Surgical ICU patients who is on slow low efficiency daily hemodiafiltration (SLEDD-f) and requires vancomycin therapy
Treatment:
Device: sustained low efficiency daily hemodiafiltration (SLEDD-f)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems