Recruiting

Observational Study

Sponsor:

UCLA

Code:

NCT01932411

Conditions

Coronary Artery Disease

Valvular Diseases

Vascular Diseases

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Study Details

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.

Conditions

Coronary Artery Disease

Valvular Diseases

Vascular Diseases

Study ID

NCT01932411

Start date

Jul, 2013

Status verified date

Feb, 2026

Completion date

Jul 1, 2026

Anticipated

Primary completion date

Jul 1, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

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.

Exclusion Criteria:

Patients that did not undergo cardiovascular surgeries and age< 18 years old will be excluded from the study.

Study Design

Enrollment

5000 participants

Anticipated

Interventions and Outcome Measures

Primary outcome measure

  • all cause mortality [ Time Frame: 12 years ]

Central Contacts and Locations

Locations

University of California Davis Health System

Recruiting

Sacramento, California, United States, 95817

Contacts

Principal Investigator:

Hong Liu, MD

More Information

Sponsor

University of California, Davis

Last update posted

Feb 12, 2026

Last verified

Feb, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of California, Davis on 2026-02-12.