Starling Registry Study

Completed

Conditions studied: Hemodynamic Monitoring

In brief

Hemodynamic optimization of critically ill patients is a goal for clinicians in order to afford the patient the best possible outcomes. Being able to precisely and rapidly determine patient fluid responsiveness provides the bedside physician and nursing staff the information needed to make critical decisions in regards to the patient's fluid status and management of additional fluids and medications. As fluid management and cardiac output determination are linked to better decision-making and improved outcomes in ICU, the use of a dynamic assessment of fluid responsiveness becomes a key tool for patient management. This study is designed to collect treatment and outcome data on patients that have undergone hemodynamic monitoring in a wide variety of clinical settings, involving a variety of patient diagnoses.

Key facts

Study ID

NCT04648293

Run by

Baxter Healthcare Corporation

People needed

1207

Starts

2020-11-16

Expected to finish

2024-02-21

Last updated by the study team

2024-04-16

Who can join

Age: 18 and older, up to 95. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• ≥18 to 95 years of age
• Patient has undergone hemodynamic monitoring with the Starling monitor
• Hemodynamic monitoring was completed no earlier than 2018

You may not qualify if…

• None

Where it is running

• Baxter Investigational Site — Denver, Colorado, United States
• Baxter Investigational Site — Quincy, Illinois, United States
• Baxter Investigational Site — Kansas City, Kansas, United States
• Baxter Investigational Site — St Louis, Missouri, United States
• Mercy Hospital St. Louis — St Louis, Missouri, United States
• Baxter Investigational Site — Camden, New Jersey, United States
• Baxter Investigational Site — Cleveland, Ohio, United States
• Baxter Investigational Site — Columbus, Ohio, United States
• Baxter Investigational SIte — Galveston, Texas, United States

Full record on ClinicalTrials.gov

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