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Suppression Of Atrial Fibrillation With Ranolazine After Cardiac Surgery

Heart; Dysfunction Postoperative, Cardiac Surgery Clinical Trial

Official title:
Suppression Of Atrial Fibrillation With Ranolazine After Cardiac Surgery

Clinical Trial Summary

The objective of this study is to show that ranolazine is a safe, viable and potent alternative for post-operative atrial fibrillation suppression in patients undergoing cardiac surgery

Clinical Trial Description

A single center, double blind, prospective, randomized study for patients who are scheduled for elective cardiac surgery (CABG, or valve or CABG and valve). All patients who meet criteria will be prospectively enrolled in a randomized fashion. Patients enrolled will be assigned to receive twice daily identical capsules containing either placebo or ranolazine. Study drug will be initiated 2 days before surgery. Patients will receive study drug throughout their hospitalization and be kept on it for a full 2 weeks post operatively. Patients will be seen in 2 weeks and receive a 30 day follow up contact visit. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01352416
Study type Interventional
Source William Beaumont Hospitals
Contact Patti Naismith, RN
Phone 248-898-8141
Email pnaismith@beaumonthospitals.com
Status Recruiting
Phase N/A
Start date September 2010
View Details
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