Clinical Trial

Alterations of the Renin-angiotensin-aldosterone System in sEptic Shock

Study acronym: ARES
Not Yet Recruiting
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Summary
Septic shock is a common and life-threatening condition associated with an in-hospital mortality rate exceeding 40%. The symptomatic management of septic shock relies primarily on vasopressor therapy, particularly norepinephrine. However, the use of high doses of norepinephrine may lead to adverse effects, prompting the search for alternative therapeutic strategies, including angiotensin II, which has recently been investigated as an adjunctive vasopressor. Indeed, alterations of the renin-angiotensin-aldosterone system (RAAS), particularly a relative deficiency of angiotensin II, have been hypothesized to occur during septic shock. However, to date, no human study has used gold-standard techniques for measuring RAAS peptides to confirm this hypothesis. Furthermore, it remains unclear whether these alterations are specific to septic shock or may also be observed in less severe infections (sepsis) or in other forms of circulatory failure, such as cardiogenic shock.
Trial Details
NCT Number NCT07721974
Lead Sponsor Assistance Publique - Hôpitaux de Paris
Conditions Septic Shock
Enrollment 320 participants
Start Date 2026-09-15
Primary Completion 2031-09 (estimated)
Study Completion 2031-10 (estimated)
Updated on ClinicalTrials.gov 2026-07-23