TerminatedNot Applicable

Hemodynamic Response During Goal Directed Fluid Therapy in the OR

Stopped: Lack of consistent reference devices

United States18 participantsStarted 2014-09

Plain-language summary

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.

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. 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

Exclusion criteria

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

What they're measuring

Dynamic Hemodynamic Response to Fluid Resuscitation

Timeframe: Up to 6 hours but not to exceed duration of surgical procedure

Trial details

NCT IDNCT02365688

SponsorMedtronic - MITG

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2015-06

Results submitted2016-03-07

View on ClinicalTrials.gov More Hemodynamic Instability trials