Registry for patients undergoing anesthesia in cardiovascular surgery
Official title: Registry of Cardiovascular Anesthesia Including the Database of Biological Signals During Anesthesia, Preoperative Assessment and Prognosis in Patients: Severance Cardiovascular Surgery Prospective (SECURE) Database
Run by Yonsei University · NCT04833751 · Data updated 2026-11-12
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 |
|---|---|
| Ages | 19 Years and up |
| Sex | All |
| Enrollment | 10000 (estimated) |
| Sponsor | Yonsei University Academic / other |
| Locations | 1 site (Seoul) |
| Status | Recruiting |
| Started | December 14, 2018 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | July 24, 2024 |
| Trial ID | NCT04833751 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 19 and older scheduled for anesthesia at a cardiovascular hospital for surgery or procedures.
✕Probably not a fit
Patients requiring emergency procedures where there is insufficient time for consent may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: Other studies have shown success in utilizing biosignal data for monitoring during anesthesia, indicating potential for this approach.
Who can join: the full rules
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 it's running
-
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
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Milrinone vs Epinephrine on TAPSE after cardiopulmonary bypass
This study tests whether milrinone or epinephrine better supports right ventricular function (TAPSE) after cardiac surgery with CPB in adults.
-
Patient-specific MRD liquid biopsy for resected NSCLC
This study tests a personalized MRD blood and bronchial washing test after surgery to see if it can signal recurrence earlier in people with resected NSCLC.
-
Autologous adipose-derived stem cell injections for knee osteoarthritis
We’re testing whether injecting a patient’s own fat-derived stem cells into the knee can help people with knee OA feel less pain and move better, compared with a standard hyaluronic acid treatment.
-
SVF cellular mix, secretome, and knee response in osteoarthritis
This study tests the cellular composition and secretome of research-only adipose-derived SVF in adults with knee OA who are already planned to receive an autologous SVF injection as part of their care.
-
2-mm subchondral drilling vs sequential 4-mm and 2-mm drilling during CARTISTEM implantation for knee cartilage defects
This study tests whether drilling the knee with a 2-mm drill alone works as well as sequential 4-mm then 2-mm drilling when combined with CARTISTEM treatment for medial knee cartilage defects.
-
Blood biomarker cohort for memory disorders in older adults
This observational cohort will collect blood samples and brain imaging data from adults 50+ with memory disorders and a small group of healthy young adults to help find biomarkers.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.