Hemodynamic Response During Goal Directed Fluid Therapy in the OR
Not Applicable
Terminated
- Conditions
- Hemodynamic Instability
- Interventions
- Procedure: Initial bolus pre-incision
- Registration Number
- NCT02365688
- Lead Sponsor
- Medtronic - MITG
- Brief 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.
- Detailed Description
Electronic and annotated observation data to support an algorithm library
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 18
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Initial bolus pre-incision Initial bolus pre-incision Initial pre-incision bolus of 500 cc of fluids with hemodynamic response recorded
- Primary Outcome Measures
Name Time Method Dynamic Hemodynamic Response to Fluid Resuscitation Up to 6 hours but not to exceed duration of surgical procedure Physiological parameters compared before and after fluid bolus for fluid resuscitation.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Duke University Medical Center
🇺🇸Durham, North Carolina, United States