Monitoring Device for Heart Surgery Patients
Physiologic Signals and Signatures With the Accuryn Monitoring System - The Accuryn Registry
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 2,500 (estimated)
- Sponsor
- Potrero Medical · Industry
This trial is looking for adult patients who are undergoing heart surgery. Participants will have their health data tracked using the Accuryn Monitoring System during their procedure and hospital stay.
You may be able to join if
- I am at least 18 years old.
- I have provided my consent to join the study.
- I am undergoing a cardiac surgical procedure.
- I will be monitored using the Accuryn Monitoring System.
You may not be able to join if
- I have advanced chronic kidney disease with an eGFR less than 20.
- I am considered unsuitable for this study by the investigator.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your EligibilityThe 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.
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