Physiologic Signals and Signatures With the Accuryn Monitoring System (The Accuryn Registry)

Completed

Conditions studied: Acute Kidney Injury, Abdominal Compartment Syndrome, Intraabdominal Hypertension, Cardiovascular Surgery

In brief

The Accuryn Registry Study is an open-ended, global, multi-center, retrospective and prospective, single-arm data collection study with an FDA cleared device. The target population are cardiovascular surgery patients. Physiologic data measurements will be collected from enrolled subjects using electronic medical records and data streams via the Accuryn Monitoring System.

Key facts

Study ID

NCT04585555

Run by

Potrero Medical

People needed

50

Starts

2017-07-10

Expected to finish

2019-11-05

Last updated by the study team

2021-02-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult (age ≥ 18).
• Monitored on the Accuryn® Monitoring System during hospital stay.
• Patient is undergoing cardiovascular surgical intervention(s).

You may not qualify if…

• The patient is unsuitable for the study, in the opinion of the investigator. This may include vulnerable patient populations such as prisoners or those detained in a penal institution.

Where it is running

• Emory University Hospital — Atlanta, Georgia, United States

Full record on ClinicalTrials.gov

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