- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01932411
Factors Affect Outcomes in Cardiovascular Surgery
Factors That Affect the Outcomes of Cardiothoracic and Vascular Surgery
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.
Study Overview
Status
Detailed Description
Identify factors that affect perioperative morbidity and mortality in patients undergoing cardiac surgery.
Here are some examples, but may not limited the following factors:
- demographic data
- perioperative medications
- comorbidity
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Hong Liu, M.D.
- Phone Number: 916-734-2949
- Email: hualiu@ucdmc.ucdavis.edu
Study Contact Backup
- Name: Sunita Randhawa
- Phone Number: 916-734-5394
- Email: srandhawa@ucdavis.edu
Study Locations
-
-
California
-
Sacramento, California, United States, 95817
- Recruiting
- University of California Davis Health System
-
Contact:
- Sunita Randhawa
- Phone Number: 916-734-5394
- Email: srandhawa@ucdavis.edu
-
Contact:
- Hong Liu, MD
- Phone Number: 916-734-5031
- Email: hong.liu@ucdmc.ucdavis.edu
-
Principal Investigator:
- Hong Liu, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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 Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
all cause mortality
Time Frame: 12 years
|
in hospital, 30 day, one year and longer
|
12 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hong Liu, M.D., University of California, Davis, Department of Anesthesiology and Pain Medicine
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 483753
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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