Factors Affect Outcomes in Cardiovascular Surgery
Factors That Affect the Outcomes of Cardiothoracic and Vascular Surgery
1 other identifier
observational
5,000
1 country
1
Brief Summary
Identify factors that contribute to perioperative morbidity and mortality in patients undergoing cardiac surgery that involves cardiopulmonary bypass. Identify factors that affect perioperative morbidity and mortality in patients undergoing cardiac surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2013
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2013
CompletedFirst Submitted
Initial submission to the registry
August 27, 2013
CompletedFirst Posted
Study publicly available on registry
August 30, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 1, 2026
February 12, 2026
February 1, 2026
13 years
August 27, 2013
February 9, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
all cause mortality
in hospital, 30 day, one year and longer
12 years
Eligibility Criteria
patients undergoing cardiovascular surgeries
You may qualify if:
- Patients greater than or equal to 18 years old that underwent cardiovascular surgery at UC Davis Medical Center from 01/01/2001 to 07/15/2013.
- Patients will only be included that underwent cardiovascular surgeries with or without cardiopulmonary bypass.
You may not qualify if:
- Patients that did not undergo cardiovascular surgeries and age\< 18 years old will be excluded from the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of California Davis Health System
Sacramento, California, 95817, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Hong Liu, M.D.
University of California, Davis, Department of Anesthesiology and Pain Medicine
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 27, 2013
First Posted
August 30, 2013
Study Start
July 1, 2013
Primary Completion (Estimated)
July 1, 2026
Study Completion (Estimated)
July 1, 2026
Last Updated
February 12, 2026
Record last verified: 2026-02