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Starling/CRRT Observational Study

Sponsored by Baxter Healthcare Corporation

About this trial

Last updated 2 years ago

Study ID

BXU578332

Status

Withdrawn

Type

Observational

Placebo

No

Accepting

18-75 Years
18 to 95 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 4 months ago

What is this trial about?

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 regard 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 during CRRT therapy.

What are the participation requirements?

Yes

Inclusion Criteria

1. ≥18 to 95 years of age.

2. Patient has undergone hemodynamic monitoring with the Starling monitor during a CRRT treatment.

3. Hemodynamic monitoring was completed no earlier than 2018

No

Exclusion Criteria

1. Patients did not have an arterial line in place during CRRT treatment

2. Patients on extracorporeal membrane oxygenation (ECMO) or left ventricular assist device (LVAD)

3. Patients with end-stage kidney disease on chronic dialysis

4. Hemodynamic monitoring with Starling did not occur during CRRT treatment

5. Data from Starling, CRRT machine, or arterial line cannot be retrieved

Locations

Location

Status