Abstract
Background
Septic shock remains a significant cause of death in critically ill patients. During septic shock, some patients will retain microcirculatory disorders despite optimal hemodynamic support (i.e., fluid resuscitation, vasopressors, inotropes). Alterations in the microcirculation are a key pathophysiological factor of organ dysfunction and death in septic shock patients. Ilomedin is a prostacyclin analog with vasodilatory effect and anti-thrombotic properties (i.e., inhibition of platelet aggregation) preferentially at the microcirculatory level. We hypothesize that early utilization of intravenous Ilomedin in septic shock patients with clinical persistence of microperfusion disorders would improve the recovery of organ dysfunction.
Methods
The I-MICRO trial is a multicenter, prospective, randomized, double-blinded, placebo-controlled study. We plan to recruit 236 adult patients with septic shock and persistent microcirculatory disorders (i.e., skin mottling or increased capillary refill time) despite hemodynamic support. Participants will be randomized to receive a 48-h intravenous infusion of either Ilomedin or placebo starting at the earliest 6 h and later 24 h after septic shock. The primary outcome will be the change (delta) of sequential organ failure assessment (SOFA) score between randomization and day 7. Secondary outcomes will include mean SOFA score during the first 7 days after randomization, mortality at day 28 post-randomization, number of ventilation-free survival days in the 28 days post-randomization, number of renal replacement therapy-free survival days in the 28 days post-randomization, number of vasopressor-free survival days in the 28 days post-randomization, and mottling score at day 1 after randomization.
Discussion
The trial aims to provide evidence on the efficacy and safety of Ilomedin in patients with septic shock and persistent microcirculatory disorders.
Trial registration
NCT NCT03788837. Registered on 28 December 2018
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Details
; Oufella, Hafid Ait 2 ; De Backer, Daniel 3 ; Duranteau, Jacques 4 ; Leone, Marc 5 ; Levy, Bruno 6 ; Rossignol, Patrick 7 ; Vicaut, Eric 8 ; Dépret, François 9 ; Depret, François; Constantin, Jean-Michel; Ait Oufella, Hafid; Dureanteau, Jacques; Gaugain, Samuel; Audart, Jules; Lefrant, Jean-Yves; Megarbane, Bruno; Pottecher, Julien; Sonneville, Romain; Rimmele, Thomas; Ichai, Carole; Vieillard, Antoine; Tran Dinh, Alexy; Aubron, Cécile; Mari, Arnaud; Labbe, Vincent; Plantefeve, Gaetan; Fedou, Anne Laure; Barraud, Damien; Gaudry, Stéphane; Nougue, Helene1 AP-HP, Saint Louis and Lariboisière University Hospitals, Department of Anaesthesiology, Critical Care Medicine and Burn Unit, Paris, France (GRID:grid.50550.35) (ISNI:0000 0001 2175 4109); INSERM UMR-S942, Institut National de la Santé et de la Recherche Médicale (INSERM), Lariboisière Hospital and INI-CRCT Network, Paris, France (GRID:grid.457369.a); Univ Paris Diderot, Paris, France (GRID:grid.7452.4) (ISNI:0000 0001 2217 0017); University of California, San Francisco, Department of Anesthesia and Perioperative Care, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811)
2 Assistance Publique - Hôpitaux de Paris (AP-HP), Hôpital Saint-Antoine, Service de Réanimation Médicale, Paris Cedex 12, France (GRID:grid.412370.3) (ISNI:0000 0004 1937 1100); Sorbonne Université, Université Pierre-et-Marie Curie, Paris 6, France (GRID:grid.462844.8) (ISNI:0000 0001 2308 1657)
3 Université Libre de Bruxelles, Intensive Care Department, CHIREC Hospitals, Brussels, Belgium (GRID:grid.4989.c) (ISNI:0000 0001 2348 0746)
4 Université Paris Sud XI, Department of Anesthesia and Intensive Care, Hôpitaux Universitaires Paris Sud, Le Kremlin Bicêtre, France (GRID:grid.5842.b) (ISNI:0000 0001 2171 2558)
5 Aix Marseille Université, Assistance Publique Hôpitaux de Marseille, Service d’Anesthésie et de Réanimation, Hôpital Nord, Marseille, France (GRID:grid.5842.b)
6 Centre Hospitalo-Universitaire de Nancy, Service de Réanimation Médicale, Vandœuvre-Lès-Nancy, France (GRID:grid.5842.b); Université de Lorraine, Nancy, France (GRID:grid.29172.3f) (ISNI:0000 0001 2194 6418)
7 Centre d’Investigation Clinique Plurithématique Pierre Drouin-INSERM CHU de Nancy, Nancy, France (GRID:grid.410527.5) (ISNI:0000 0004 1765 1301); Université de Lorraine, FCRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists) Network, Nancy, France (GRID:grid.29172.3f) (ISNI:0000 0001 2194 6418)
8 Université Paris-Diderot, Sorbonne-Paris Cité, Fernand Widal Hospital, APHP, Department of Biostatistics, Paris, France (GRID:grid.7452.4) (ISNI:0000 0001 2217 0017)
9 AP-HP, Saint Louis and Lariboisière University Hospitals, Department of Anaesthesiology, Critical Care Medicine and Burn Unit, Paris, France (GRID:grid.50550.35) (ISNI:0000 0001 2175 4109); INSERM UMR-S942, Institut National de la Santé et de la Recherche Médicale (INSERM), Lariboisière Hospital and INI-CRCT Network, Paris, France (GRID:grid.457369.a); Univ Paris Diderot, Paris, France (GRID:grid.7452.4) (ISNI:0000 0001 2217 0017)




