Hemodynamic Response During Goal Directed Fluid Therapy in the OR

Stopped early · Not applicable

Conditions studied: Hemodynamic Instability

In brief

The purpose of this study is to retrospectively evaluate the hemodynamic response to goal directed fluid therapy fluid during open abdominal surgery where goal directed fluid therapy is a standard of care after establishing a pre-incision baseline response to fluids.

Key facts

Study ID

NCT02365688

Run by

Medtronic - MITG

People needed

18

Starts

2014-09-01

Expected to finish

2015-06-01

Last updated by the study team

2017-07-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adults ≥18 years booked for an open abdominal procedure
• American Society of Anaesthesiologists (ASA) Physical Status 1 - 3
• Expected duration of surgical procedure to be ≥ 2 hours
• Standard of care monitoring to include cardiac output

You may not qualify if…

• Open chest surgical procedure expected
• Cardiac arrhythmia such as atrial fibrillation.
• Right Ventricular Failure
• Aortic regurgitation

Where it is running

• Duke University Medical Center — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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