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RECRUITING
NCT06471231
PHASE4

Renal Outcomes in the Early Use of Vasopressin in the Treatment of Septic Shock

Sponsor: Azienda Usl di Bologna

View on ClinicalTrials.gov

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

Interventions

DRUG

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.

DRUG

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