Augmented Vs. Normal Renal Replacement Therapy in Severe Acute Renal Failure (ARF).

NCT00221013 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 1508

Last updated 2009-02-27

No results posted yet for this study

Summary

This study seeks to determine if increasing the dose of continuous renal replacement therapy (CRRT) reduces 90-day all cause mortality in Intensive Care Unit (ICU) patients with severe acute renal failure (ARF).

Conditions

  • Acute Renal Failure

Interventions

PROCEDURE

"augmented" CRRT regimen

We randomly assigned critically ill patients with acute kidney injury to receive CRRT in the form of post-dilution continuous veno-venous hemodiafiltration (CVVHDF) at 25 ml/kg/hr (lower intensity) or 40 ml/kg/hr (higher intensity) of effluent flow.

Sponsors & Collaborators

  • ANZICS Clinical Trials Group

    collaborator NETWORK
  • The George Institute

    lead OTHER

Principal Investigators

  • Prof Rinaldo Bellomo, MD · Austin Hospital, Melbourne Australia

  • Alan Cass, MD · The George Institute

  • Simon Finfer, MD · Royal North Shore Hospital

  • Carlos Scheinkestel, MD · The Alfred

  • Robyn Norton, MD · The George Institute

  • John Myburgh, MD · St George Hospital (Sydney)

  • Louise Cole, MD · Nepean Blue Mountains Local Health District

  • Martin Gallagher, MD · The George Institute

  • Shay McGuinness, MD · Auckland City Hospital CVICU

  • Colin McArthur, MD · Auckland City Hospital DCCM

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-11-30
Primary Completion
2008-10-31
Completion
2009-01-31

Countries

  • Australia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00221013 on ClinicalTrials.gov