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Intravenous Lidocaine and Postoperative Outcomes After Cardiac Surgery

Atrial Fibrillation Clinical Trial

Official title:
The Effect of Perioperative Intravenous Lidocaine on Postoperative Outcomes After Cardiac Surgery

Clinical Trial Summary

This study is being done to determine if lidocaine, administered during surgery and for 24 hours after surgery can reduce inflammation, thereby reducing the risk of atrial fibrillation and 30 day mortality after surgery. Participants undergoing cardiac surgery will be randomized to receive either lidocaine or placebo.

Clinical Trial Description

Subjects undergoing cardiac surgery are randomized into one of two groups.

- Group 1: Intravenous Lidocaine Group

- Group 2: Intravenous placebo Group

Either Lidocaine or placebo is administered throughout surgery and 24 hours after surgery.

Patients in both groups will undergo quality of life assessments and functional recovery assessments post-surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00840918
Study type Interventional
Source The Cleveland Clinic
Contact
Status Terminated
Phase N/A
Start date February 2009
Completion date December 15, 2014
View Details
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