Critical Illness Clinical Trial
Official title:
Sup-Icu RENal (SIREN) - a Sub-analysis of the Prospective SUP (Stress Ulcer Prophylaxis)-ICU Trial on the Risk of GI- Bleeding in ICU Patients Receiving Renal Replacement Therapy
Data show that episodes of bleeding may often be observed in critically ill patients with
dialysis-dependent acute renal failure (ARF) on renal replacement therapy (RRT). From a
clinical perspective, patients with dialysis-dependent ARF and end-stage renal disease (ESRD)
may be considered a high risk population in regard to e.g. development of gastrointestinal
(GI-) bleeding.
In the current prospective subanalysis "SIREN" of the randomized placebo-controlled clinical
trial "SUP-ICU" (NCT02467621), the investigators seek to elucidate whether the subpopulation
of critically ill patients with acute kidney injury requiring renal replacement therapy (RRT)
benefit from prophylactic treatment with a proton-pump-inhibitor such as pantoprazole.
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