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N/A N=18

Observational Study of Citrate Based Dialysis in Pediatric Patients Receiving Hemodialysis

Complication of Dialysis

Enrolled (actual)
18
Serious AEs
0.0%
Results posted
Mar 2016
Primary outcome: Primary: Dialyzer Clotting Rate — 6 percentage of total treatments

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Use of citrate based dialysate (Procedure)
Age
Pediatric, Adult · 0+ yrs
Sex
All
Sponsor
Loma Linda University
Primary completion
Jan 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Dialyzer Clotting Rate
6
SECONDARY
Saline Flush Rate
SECONDARY
Heparin Use Rate

Summary

Providing hemodialysis requires the use of an extracorporeal circuit which must be anticoagulated. Inadequate anticoagulation can result in the dialyzer clotting with decreased circuit blood flows, inefficient dialysis and even significant blood loss secondary to circuit clotting.Heparin has been traditional agent used to provide anticoagulation. Heparin has multiple adverse side effects that would be best avoided in acutely ill patients who are at risk for bleeding. Alternative means of providing anticoagulation include citrate based anticoagulation. Citrasate® is a heparin free anticoagulant alternative that has been FDA approved since 1999 and readily available for commercial use since 2001. Citrasate® utilizes citric acid instead of acetic acid for acidification; the presence of small amounts of citrate in the dialysate also provides the means for anticoagulation. The concentration of citrate is low (2.4meq/L) and thus has a minimal effect on serum calcium values. No calcium monitoring or infusion is indicated. The purpose of this study is to obtain further data on the use of Citrasate® in admitted pediatric patients who receive hemodialysis as part of their therapy for acute kidney injury.

Eligibility Criteria

Inclusion Criteria

  • All pediatric patients between the ages of 0-21 years in the inpatient setting requiring hemodialysis for renal replacement therapy. These will include both patients with chronic renal failure and acute kidney injury, or any patient requiring dialysis as determined by an attending nephrologist.

Exclusion Criteria

  • Symptomatic hypocalcemia that is refractory to treatment 24 hours prior to the start of each dialysis session
  • Known liver disorder/acute liver failure with an inability to metabolize citrate.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01590550). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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