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CompletedNCT00529139

Hannover Dialysis Outcome Study

The Hannover-Dialysis-Outcome (HAN-D-OUT)-Study: Comparison of Standard Versus Intensified Extended Dialysis in Treatment of Patients With Acute Kidney Injury in the Intensive-Care Unit

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
157 (actual)
Sponsor
Hannover Medical School · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Mortality rates of patients with acute kidney injury in the intensive care unit have changed little over the past few decades despite significant advances in supportive care. Few interventions have been shown to result in an improvement of in-hospital mortality of these patients, with dose of renal replacement therapy (RRT) being one of the most important. Patients undergoing continuous veno-venous hemofiltration had better outcomes with ultrafiltration rates of 35 mL/kg/h or 45 mL/kg/h than those treated at a rate of 20 mL/kg/h. In a different trial, intermittent hemodialysis on a daily basis resulted in better control of uremia, fewer hypotensive episodes during dialysis, and more rapid resolution of acute renal failure than thrice weekly hemodialysis. In the present study we examine survival and renal recovery in critically ill patients with acute kidney injury that are treated with a currently recommended (standard) dose of RRT, and patients that receive intensified RRT.

Conditions

Interventions

TypeNameDescription
DEVICEStandard extended dialysisStandard extended dialysis dosed to maintain plasma urea levels between 120-150 mg/dL (20 -25 mmol/L)
DEVICEIntensified extended dialysisIntensified extended dialysis dosed to maintain near-normal plasma urea levels, i.e. \<90 mg/dL (\<15 mmol/L)

Timeline

Start date
2003-07-01
Completion
2006-05-01
First posted
2007-09-14
Last updated
2007-09-17

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00529139. Inclusion in this directory is not an endorsement.

Hannover Dialysis Outcome Study (NCT00529139) · Clinical Trials Directory