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Biobank Cardiac Surgery

Biobank of Blood and Tissue Samples From Patients Undergoing Cardiac Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06747806
Enrollment
500
Registered
2024-12-24
Start date
2023-12-18
Completion date
2028-12-31
Last updated
2025-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases

Brief summary

Treatment strategies for cardiac surgery patients have been evolving significantly for the last decade. While clinical outcomes have been improving, there are still significant areas unexplored in these patients. Cardiac surgery, or cardiovascular surgery, is surgery on the heart or great vessels performed by cardiac surgeons. It is often used to treat complications of ischemic heart disease (for example, with coronary artery bypass grafting); to correct congenital heart disease; or to treat valvular heart disease from various causes, including endocarditis, rheumatic heart disease, and atherosclerosis. Biobanking is a fundamental process required in the better understanding of human diseases together with their underlying mechanisms. Biobanking refers to the process by which samples of bodily fluid or tissue are collected for research use to improve the understanding of health and disease. For this study, the investigator's objective is to acquire elucidation in disease etiology, translation, and advancing public health by evaluating blood and tissue results of those with cardiac disease undergoing cardiac surgery.

Interventions

PROCEDURECardiac Surgery and Procedures

To assess blood and tissue biomarkers of patients undergoing cardiac surgery

Sponsors

University of Chicago
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients who undergo cardiac surgery at Advocate Children's Hospital (ACH)& University of Chicago Medical Center (UCMC) by the ACH & UC Cardiothoracic Surgery Research team who are pediatric neonates and up. * Patients will only be English speaking.

Exclusion criteria

* Vulnerable Subjects/Subject Capacity to provide consent

Design outcomes

Primary

MeasureTime frameDescription
Concentration of the elucidation in disease etiology from evaluating blood and tissue resultsFrom date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 monthsTo acquire elucidation in disease etiology health by evaluating blood and tissue results of those with cardiac disease undergoing cardiac surgery.
Concentration of the elucidation in disease translation from evaluating blood and tissue resultsFrom date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 monthsTo acquire elucidation in disease translational health by evaluating blood and tissue results of those with cardiac disease undergoing cardiac surgery.
Concentration of the elucidation in advancing public health by evaluating blood and tissue resultsFrom date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 monthsTo acquire elucidation in advancing public health by evaluating blood and tissue results of those with cardiac disease undergoing cardiac surgery.

Countries

United States

Contacts

Primary ContactValluvan Jeevanandam, MD
jeevan@bsd.uchicago.edu7738345087
Backup ContactLeila Yazdanbakhsh
leila.yazdanbakhsh@bsd.uchicago.edu7738345087

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026