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Clinical Trial Summary

The purpose of this study is to assess the effect of a higher mean arterial pressure on renal function for patients with shock and elevated central venous pressure.


Clinical Trial Description

Current recommandation for mean arterial pressure (MAP) target is 65 mmHg for septic shock, but optimal target to prevent acute renal failure (ARF) remains unknown. High central venous pressure (CVP) can lead to acute renal failure through venous congestion , and is associated with acute renal failure in intensive care unit. A decrease of renal perfusion pressure, defined by MAP - CVP, has been shown to be associated with risk of acute renal failure. The main objective of this trial is to evaluate if an optimisation of renal perfusion pressure, by a higher MAP when CVP is high (≥ 12 cmH2O), can improve renal function. In this interventional monocenter trial, each patient will be evaluated during 2 consecutive periods of 6 hours, with a temporary MAP target - Target at 65-70mmHg during 6 hours - Target at 80-85mmHg during 6 hours Patients will be randomized into two groups to define the order of targets. There will be a stratification on previous arterial hypertension. Renal function will be measured at the end of each period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05655065
Study type Interventional
Source University Hospital, Angers
Contact Nicolas FAGE, MD
Phone +332 41 35 36 37
Email nicolas.fage@chu-angers.fr
Status Not yet recruiting
Phase N/A
Start date January 2023
Completion date December 31, 2026

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