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

Description

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.

Conditions

Intraabdominal Hypertension, Abdominal Compartment Syndrome, Acute Kidney Injury, Cardiovascular Surgery

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Study Overview

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Study Details

Study overview

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.

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

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

Condition
Intraabdominal Hypertension
Intervention / Treatment

-

Contacts and Locations

Los Angeles

Cedars-Sinai Medical Center, Los Angeles, California, United States, 90048

San Francisco

San Francisco VA Medical Center, San Francisco, California, United States, 94121

Washington

George Washington University Hospital, Washington, District of Columbia, United States, 20037

Weston

Cleveland Clinic Florida, Weston, Florida, United States, 33331

Louisville

Jewish Hospital / University of Louisville, Louisville, Kentucky, United States, 40202

Asheville

Mission Health Hospital, Asheville, North Carolina, United States, 28803

Durham

Duke University Hospital, Durham, North Carolina, United States, 27710

Winston-Salem

Wake Forest Baptist Medical Center, Winston-Salem, North Carolina, United States, 27157

Cleveland

Cleveland Clinic, Cleveland, Ohio, United States, 44195

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Signed or Verbal Informed Consent as required by IRB (if applicable).
  • 2. Adult (age ≥ 18).
  • 3. Monitored on the Accuryn® Monitoring System during their procedure and ICU stay (for retrospective enrollment).
  • 4. Patient is undergoing cardiac surgical intervention(s).
  • 1. Known history of advanced chronic kidney disease defined by an estimated glomerular filtration rate (eGFR) \<20 mL/min/1.73m2 within 30 days prior to procedure.
  • 2. The patient is unsuitable for the study, in the opinion of the investigator. This may include vulnerable patient populations such as pregnant women, prisoners ,or those detained in a penal institution.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Potrero Medical,

Vanessa Moll, MD, PhD, STUDY_DIRECTOR, Potrero Medical

Study Record Dates

2026-12-31