Hemodynamic Response During Goal Directed Fluid Therapy in the OR

Medtronic

Status: Terminated

Conditions: Hemodynamic Instability

Treatments: Procedure: Initial bolus pre-incision

Study type: Interventional

Funder types: Industry

Identifiers

NCT02365688

COVMOPR0436

Details and patient eligibility

About

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.

Full description

Electronic and annotated observation data to support an algorithm library

Enrollment: 18 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

1. Open chest surgical procedure expected
2. Cardiac arrhythmia such as atrial fibrillation.
3. Right Ventricular Failure
4. Aortic regurgitation

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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18 participants in 1 patient group

Initial bolus pre-incision

Other group

Description:

Initial pre-incision bolus of 500 cc of fluids with hemodynamic response recorded

Treatment:

Procedure: Initial bolus pre-incision