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Clinical Trial Summary

Norepinephrine is a catecholamine that is the first-line vasopressor for septic shock. The addition of non-catecholamine vasopressors, including vasopressin and angiotensin-II may be used in adults with septic shock that have inadequate mean arterial pressure while on norepinephrine. Uncertainty exists regarding the timing of initiation of these agents and there is a lack of data comparing their safety and efficacy. The current literature suggests that earlier initiation of angiotensin-II will have a more significant reduction on norepinephrine-equivalent dose compared to later initiation. In addition, approximately half of patients initiated on vasopressin do not have an early hemodynamic response 6 hours after initiation. The purpose of this study is to evaluate the efficacy of angiotensin-II when used as the second vasopressor agent for septic shock.


Clinical Trial Description

Objectives: Primary Objective: 1. To evaluate the efficacy of ang-II when used as the second vasopressor agent for septic shock Secondary Objectives: 1. To assess the duration of response to ang-II 2. To assess overall survival 3. To assess the amount of time spent in the ICU 4. To assess the need for renal replacement therapy 5. To assess the overall duration of vasoactive medication use 6. To assess toxicity and tolerability ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06122987
Study type Interventional
Source Kingman Regional Medical Center
Contact Tyson Dietrich, PharmD
Phone 928-263-3933
Email TDietrich@azkrmc.com
Status Recruiting
Phase Phase 4
Start date December 4, 2023
Completion date January 2025

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