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A Prospective Multi-Center Randomized Open-Label Study To Evaluate The Efficacy and Safety of PMX Cartridge in addition to Standard Medical Care for Patients with Endotoxemic Septic Shock: TIGRIS TRIAL

Primary Objective

The primary objective is to compare the safety and efficacy of the PMX cartridge (Toraymyxin) based on mortality at 28 days in patients with septic shock and endotoxemia who are treated with standard medical care plus the use of the PMX cartridge, versus patients who receive standard medical care alone.

Study

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Details
Age

Adult

Type of Study

Device Feasibility

Scope

National

Location

Memorial Hospital Central

Principal Investigator
Ronald Rains

Ronald Rains

Study ID

Protocol Number: 19-6070

More information available at ClinicalTrials.gov: NCT03901807

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