RecruitingIntraabdominal HypertensionAbdominal Compartment SyndromeAcute Kidney Injury
Physiologic Signals and Signatures With the Accuryn Monitoring System - The Accuryn Registry
Eligible age
18+ yrs
Accepts
All genders
Locations
6 states
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
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.
Sponsor: Potrero Medical
You may qualify if…
- ✓ 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).
You may not qualify if…
- ✕ 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.
Where it's recruiting
California
Los Angeles · San Francisco
District of Columbia
Washington D.C.
Florida
Weston
Kentucky
Louisville
North Carolina
Asheville · Durham · Winston-Salem
Ohio
Cleveland
Source: ClinicalTrials.gov · NCT04669548 · last updated 2022-09-28