Overview

Dopexamine and Norepinephrine Compared With Epinephrine Alone in Septic Shock

Status:
Completed
Trial end date:
2004-06-01
Target enrollment:
0
Participant gender:
All
Summary
In septic shock, when volume resuscitation fails to restore mean arterial pressure, catecholamines such as dopamine, dobutamine, epinephrine, or norepinephrine are used, either alone or in combination. Although they allow hemodynamic success to be obtained, they can leave some regional blood flows impaired, especially the hepatosplanchnic perfusion, which contributes to multiple organ failure. Dopexamine is a structural and synthetic analog of dopamine that exerts systemic and gut vasodilation and stimulates cardiac contraction. In experimental models, dopexamine has been shown to exert anti-inflammatory properties and to protect the hepatic ultra structure. The combination of dopexamine and norepinephrine could therefore constitute an interesting alternative in treating septic shock patients. This study will test the efficacy (on gastric mucosal blood flow, hepatic damage and oxidative stress) and safety of the combination of dopexamine and norepinephrine (compared to those of epinephrine alone) in the treatment of patients with septic shock.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Rennes University Hospital
Treatments:
Dopamine
Dopexamine
Epinephrine
Epinephryl borate
Norepinephrine
Racepinephrine
Criteria
Inclusion Criteria:

- Adults over 18 years

- Informed consent

- Septic shock with:

- evidence of infection;

- at least 3 of the following criteria: temperature > 38°C or < 36.5°C; respiratory
rate > 20 breaths per minute or PaCO2 < 32 mmHg or mechanical ventilation; heart
rate > 90 beats/min; white blood cell count > 12,000/mm3 or < 4,000/mm3;

- at least 2 of the following criteria: plasma lactate > 2 mmol/L or unexplained
metabolic acidosis (pH < 7.3); hypoxemia defined by PaO2 < 70 mmHg at room air or
a PaO2/FiO2 ratio < 280 mmHg (or < 200 mmHg if pneumonia was the source of
sepsis) or need for mechanical ventilation; urine output < 30 mL/h for at least 2
hours despite a fluid challenge of at least 500mL; a platelet count <
100,000/mm3, a decrease of 50% from previous value, or unexplained coagulopathy
(prothrombin time < 60% and elevated fibrin degradation products > 10 μg/mL);

- systolic blood pressure < 90 mmHg despite an optimal volume loading defined by a
pulmonary capillary wedge pressure > 12 mmHg.

Exclusion Criteria:

- Pregnant women

- Patients with a history of esophageal or gastric disease

- Patients with a history of esophageal or gastric surgery