Performance of Non-Invasive Monitors During ANH

Withdrawn before enrolling

Conditions studied: Baseline, Hemodilution

In brief

The aim of this study is to assess the responsiveness of the standard minimally invasive hemodynamic monitors used in the operating room to known changes in the intravascular volume status that occur during blood removal and volume replacement with three different standard fluids used during ANH.

Key facts

Study ID

NCT02179827

Run by

University of California, Davis

People needed

0

Starts

2022-11-01

Expected to finish

2024-11-01

Last updated by the study team

2022-04-27

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Those surgical procedures where ANH is included in the surgical plan and consent is obtained

You may not qualify if…

• Severe or symptomatic COPD, emphysema, renal, hepatic or coronary artery disease as defined by the American College of Cardiology (Cannon et al., 2001).
• Esophageal pathology (diverticulum, hiatal hernia, esophageal cancer, esophageal surgery), which introduces risks associated with the placement of the esophageal Doppler.
• Ascites.
• BMI >35
• Pregnancy

Where it is running

• UC Davis Health System — Sacramento, California, United States

Full record on ClinicalTrials.gov

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