The Effect of Perioperative Medications on the Outcomes of Patients Undergoing Cardiac Surgery

Completed

Conditions studied: Cardiac Diseases

In brief

This study will be a retrospective study. The patient data from the electronic medical records and existing database will be collected and analyzed. Primary endpoints will be postoperative mortality (within 30 days) and overall complications and length of hospital stay. The secondary endpoints will be myocardial infarction, cardiac death, CHF, arrhythmia, ischemia, stroke, neurological complications, length of ICU stay, re-admission rate, infections, pulmonary complications, length of intubation time, length of ventilation time, and acute renal failure.

Key facts

Study ID

NCT01683448

Run by

University of California, Davis

People needed

1

Starts

2010-02-01

Expected to finish

2015-02-01

Last updated by the study team

2020-12-03

Who can join

Age: 18 and older, up to 89. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• All cardiac surgical patients

You may not qualify if…

• Non cardiac surgery

Where it is running

• UC Davis, Medical Center — Sacramento, California, United States

Full record on ClinicalTrials.gov

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