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OpenTrials
Completed

NCT Number: NCT01995786

Clinical Outcomes and Costs Analyses in Use of Goal Directed Therapy

The aim of the study is to evaluate clinical and economic impact of Goal Directed Fluid Therapy according to NICE haemodynamic protocol. Haemodynamic parameters were assessed using automated pulse contour analysis (Flotrac/Vigileo®). A specific dedicated software has been developed to perform clinical and expenditures data collection, both retrospective and prospective data are archived.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Regina Elena CI

Rome, Italy, 00144

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients selected for major abdominal surgery

Exclusion criteria

•Patients under the age of 18, patients with hemodynamically significant aortic regurgitation and heart rhythm disorders

Treatment and study plan

Goal Directed Fluid Therapy FloTrac/Vigileo

Device

Primary outcomes

  1. rate of reduction of postoperative spending

    Time frame: 30 day postoperative

Sponsors and collaborators

Lead sponsor

Regina Elena Cancer Institute

Other

Registry information

Important dates

Study start
2012
Primary completion
2014
First posted
Nov 27, 2013
Registry last updated
Apr 7, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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