Fluid Oriented Therapy During Major Abdominal Surgery
Not Applicable
Completed
- Conditions
- Goal Directed Therapy
- Interventions
- Device: FloTrac
- Registration Number
- NCT03023618
- Brief Summary
In this "before and after" study we will investigate the potential benefit on postoperative outcomes of a guided fluid therapy with a stroke volume optimization . The NICE protocol has been applied by means of EV1000 monitor and arterial waveform analysis ( Flotrac - Edwards). In the postoperative period overall complications, as well as exitus , will be analyzed and compared with those of a control group underwent the same surgical interventions, with a standard hemodynamic monitoring.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 180
Inclusion Criteria
- ASA 1-2 patients
Exclusion Criteria
- Severe Caridiac Disease
- Renal Failure
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description case group FloTrac patients after 2014, after management of fluid therapy has been guided by FloTrac parameters as a standard clinical practice (NICE protocol)
- Primary Outcome Measures
Name Time Method complication rate up to 30 days postoperatively
- Secondary Outcome Measures
Name Time Method Duration of hospitalization an average of 30 days