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RECRUITING
NCT04669548

Physiologic Signals and Signatures With the Accuryn Monitoring System - The Accuryn Registry

Sponsor: Potrero Medical

View on ClinicalTrials.gov

Summary

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.

Official title: Physiologic Signals and Signatures With the Accuryn Monitoring System - A Retrospective and Prospective Analysis (The Accuryn Registry)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

2500

Start Date

2020-12-21

Completion Date

2026-12-31

Last Updated

2022-09-28

Healthy Volunteers

No

Interventions

DEVICE

Accuryn Monitoring System

The Accuryn Monitoring System is a novel Foley catheter and monitoring device capable of detecting physiologic changes in vital signs via sensors within the catheter system. These data are captured non-invasively, continuously, and at a high frequency.

Locations (9)

Cedars-Sinai Medical Center

Los Angeles, California, United States

San Francisco VA Medical Center

San Francisco, California, United States

George Washington University Hospital

Washington D.C., District of Columbia, United States

Cleveland Clinic Florida

Weston, Florida, United States

Jewish Hospital / University of Louisville

Louisville, Kentucky, United States

Mission Health Hospital

Asheville, North Carolina, United States

Duke University Hospital

Durham, North Carolina, United States

Wake Forest Baptist Medical Center

Winston-Salem, North Carolina, United States

Cleveland Clinic

Cleveland, Ohio, United States