Fluid Oriented Therapy During Major Abdominal Surgery

Not Applicable

Completed

• Conditions: Goal Directed Therapy

• Registration Number: NCT03023618
• Lead Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS

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

Study Timeline

• Study Start: 2012-01
• Primary Completion: 2016-05
• Study Completion: 2016-05
• Status Verified: 2017-01
• Study First Submitted: 2017-01-01
• Study First Submitted QC: 2017-01-17
• Last Update Submitted: 2017-01-17
• Study First Posted: 2017-01-18
• Last Update Posted: 2017-01-18

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

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