Patients with acute abdomen in which to proceed is necessary to intervention in regime of urgency. MedDRA version: 9.1 Level: SOC Classification code 10042613
Conditions
Interventions
Pharmaceutical Form: Solution for infusion
INN or Proposed INN: Electrolytes
Concentration unit: mEq/l milliequivalent(s)/litre
Concentration type: equal
Concentration number: 154-
Sponsors
U.O. Terapia Intensiva
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients with acute abdomen undergoing abdominal surgery on an urgent and present on arrival in type at least one sign of ipoperfusione. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: Patients with chronic renal failure already undergoing dialysis treatment. SCA 5 units of EC) Patients with values of ≥ 5 PVC mmHg Patients on the list for OLT Patients with age less than 18 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: Objective of the study is to evaluate differences between two groups treated with different fluidic strategy in terms of mortality at thirty days;Secondary Objective: Secondary objectives are to evalaute differences between two groups treated with different strategy in terms of fluidic surgical complications, onset of organ failure, duration of mechanical ventilation and length of stay in intensive care.;Primary end point(s): 1.Mortality to 30 days | — |
Countries
Italy
Outcome results
None listed