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Clinical Trials/NCT03023618
NCT03023618
Completed
Not Applicable

Effect Of Stroke Volume Optimization On Complication Rate Of Patients Undergoing Pancreatic Surgery

Fondazione Policlinico Universitario Agostino Gemelli IRCCS0 sites180 target enrollmentJanuary 2012
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ConditionsGoal Directed Therapy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Goal Directed Therapy
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Enrollment
180
Primary Endpoint
complication rate
Status
Completed
Last Updated
9 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
May 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr.Andrea Russo

Principal investigator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Eligibility Criteria

Inclusion Criteria

  • •ASA 1-2 patients

Exclusion Criteria

  • •Severe Caridiac Disease
  • •Renal Failure

Outcomes

Primary Outcomes

complication rate

Time Frame: up to 30 days postoperatively

Secondary Outcomes

  • Duration of hospitalization(an average of 30 days)

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