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Renal Outcomes in the Early Use of Vasopressin in the Treatment of Septic Shock
Sponsor: Azienda Usl di Bologna
Summary
The aim of the present study is to verify whether the earlier association of vasopressin and norepinephrine, in patients in septic shock, determines variations in terms of use of renal function replacement techniques in the first 7 days of hospitalization in Intensive Care, compared to patients in whom vasopressin is added only when norepinephrine reaches a higher dose.
Key Details
Gender
All
Age Range
18 Years - 80 Years
Study Type
INTERVENTIONAL
Enrollment
264
Start Date
2024-05-15
Completion Date
2026-05-15
Last Updated
2024-06-24
Healthy Volunteers
No
Conditions
Interventions
vasopressin infusion when the norepinephrine dosage is equal to or greater than 0.25 mcg/kg/min
when the norepinephrine dosage is equal to or greater than 0.25 mcg/kg/min in the absence of adequate MAP (Mean arterial pressure \>65 mmhg), vasopressin infusion will be associated with the standard dosage of 0.3UI/min.
vasopressin infusion when the norepinephrine dosage is equal to or greater than 0.5 mcg/kg/min
the infusion of vasopressin at a dosage of 0.3 IU/min will be associated if norepinephrine exceeds the dosage of 0.5 mcg/kg/min in the absence of adequate MAP
Locations (1)
Azienda Unità Sanitaria Locale
Bologna, Italy