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Simultaneous Administration of Norepinephrine, Angiotensin II, and Vasopressin in Septic Shock Patients
The goal of this prospective randomized controlled trial is to compare the effects of classic stepwise vs. early balanced multimodal vasopressor strategies in septic shock.
CONTROL GROUP(Classic stepwise vasopressor administration): Patients will be started on norepinephrine with increases of 0.05-0.1 mcg/kg/min up to 0.5 mcg/kg/min, followed by vasopressin (administered at a fixed dose of 0.03 IE/min). If MAP remains \< 65 mmHg, norepinephrine will be titrated above dose of 0.5 mcg/kg/min until MAP ≥ 65 mmHg. Initiation of additional vasoactive drugs (epinephrine, Ang II, methylene blue or dopamine) as per clinical team decision. Initiation of inotropes (dobutamine, milrinone, levosimendan) as per clinical team decision. EXPERIMENTAL GROUP(Balanced multimodal vasopressor administration): Early, simultaneous start of norepinephrine, angiotensin II and vasopressin at equivalent starting doses (equivalent to approximately 0.05 mcg/kg/min of norepinephrine). Increments of 0.05 mcg/kg/min of equivalent doses of all three vasopressors every 3-5 min until MAP ≥ 65 mmHg is reached (vasopressin will be administered at a maximum dose of 0.03 IE/min, Ang II will be administered at maximum dose of 100ng/kg/min). Initiation of additional vasoactive drugs (epinephrine, methylene blue or dopamine) as per clinical team decision. Initiation of inotropes (dobutamine, milrinone, levosimendan) as per clinical team decision.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University Hospital Centre Zagreb
Zagreb, Croatia
Medical intensive care unit UMC Maribor
Maribor, Slovenia
Start Date
December 23, 2023
Primary Completion Date
December 1, 2025
Completion Date
November 1, 2026
Last Updated
July 3, 2025
80
ESTIMATED participants
Simultaneous administration of vasopressors
OTHER
Successive administration of vasopressors
OTHER
Lead Sponsor
University Medical Centre Maribor
NCT06043505
NCT05688774
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