Personalized Mean Arterial Pressure Management on Renal Function During Septic Shock (DORESEP)
Septic Shock, Acute Kidney Injury
About this trial
This is an interventional treatment trial for Septic Shock focused on measuring Sepsis, Acute kidney injury, Mean arterial pressure, Catecholamines, Renal doppler
Eligibility Criteria
Inclusion Criteria:
- Any patient with septic shock may be included in the next 6 to 16h
- Age > 18 years old and <= 80 years
Exclusion Criteria:
- Chronic renal failure (Baseline serum creatinine > 120 mmol/L)
- Chronic cardiac failure (Left ventricle ejection fraction < 40%)
- Pregnancy
- Urinary Tract Infection
- Patients with a left ventricular dysfunction ( ventricular ejection fraction <40%)
Sites / Locations
- Reanimation Chirurgicale - Hôpital Kremlin Bicêtre
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Test group
Control group
Patients will be treated with fluid and norepinephrine to achieve and maintain a mean arterial pressure of 65 mm Hg. Then they will be randomized in two groups. In the first group (study group, n=30), mean arterial pressure will be increased to 85 mm Hg for 72 hours by increasing the dose of norepinephrine in patients (A maximum dose of 1.2 mcg / kg / min is not exceeded). Key details, e.g., for drugs include dosage form, dosage, frequency and duration.
Patients will be treated with fluid and norepinephrine to achieve and maintain a mean arterial pressure of 65 mm Hg. Then they will be randomized in two groups. In this group (control group, n=30), mean arterial pressure will be maintained at 65 mm Hg.