Prevention of Postoperative Atrial Fibrillation

NCT01742039 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 160

Last updated 2023-10-13

No results posted yet for this study

Summary

The primary aim of this study is to determine the safest and most effective therapeutic strategy to decrease the incidence of postoperative atrial fibrillation following cardiac surgery in an era with shorter ICU and hospital length of stay. A secondary goal is to evaluate the length of hospital stay associated with each treatment strategy.

Conditions

  • Postoperative Atrial Fibrillation

Sponsors & Collaborators

  • George Washington University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-07-31
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01742039 on ClinicalTrials.gov