Registry for patients undergoing anesthesia in cardiovascular surgery
Registry of Cardiovascular Anesthesia Including the Database of Biological Signals During Anesthesia, Preoperative Assessment and Prognosis in Patients: Severance Cardiovascular Surgery Prospective (SECURE) Database
This study is trying to gather information from patients who have anesthesia during heart surgeries to improve anesthesia care and outcomes for future patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 10000 (estimated) |
| Ages | 19 Years and up |
| Sex | All |
| Sponsor | Yonsei University Academic / other |
| Locations | 1 site (Seoul) |
| Trial ID | NCT04833751 on ClinicalTrials.gov |
What this trial studies
This study aims to create a comprehensive registry database for patients receiving anesthesia during cardiovascular surgeries. It will collect detailed preoperative assessments, perioperative biosignal data, and hemodynamic information, along with medication usage and prognosis from electronic medical records. The goal is to develop a monitoring system that integrates multiple biosignal data to enhance anesthesia care and patient outcomes.
Who should consider this trial
Good fit: Ideal candidates are adults aged 19 and older scheduled for anesthesia at a cardiovascular hospital for surgery or procedures.
Not a fit: Patients requiring emergency procedures where there is insufficient time for consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this could lead to improved anesthesia management and better outcomes for patients undergoing cardiovascular procedures.
How similar studies have performed: Other studies have shown success in utilizing biosignal data for monitoring during anesthesia, indicating potential for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Adults age 19 and older 2. Patients scheduled for anesthesia at a cardiovascular hospital for cardiovascular surgery or procedures Exclusion Criteria: 1\) Emergency (surgery/procedure room transfer within 1 hour of visit) where there is insufficient time for the subject (adult 19 years of age or older) or his/her representative (adult incapable of consent) to decide whether to participate in the study
Where this trial is running
Seoul
- Yonsei University Health System, Severance Hospital — Seoul, South Korea (Recruiting)
Study contacts
- Principal investigator: Sarah Soh, MD, PhD — Department of Anesthesiology and Pain Medicine, Yonsei Cardiovascular Hospital, Yonsei University College of Medicine
- Study coordinator: Sarah Soh, MD, PhD
- Email: yeonchoo@yuhs.ac
- Phone: 82-2-2228-8512
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.