Intraoperative Epiaortic Scanning for Preventing Early Stroke After Off-pump Coronary Artery Bypass

Coronary Artery Occlusive Disease Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01764763
• Other study ID #: 4-2010-0868
• Status: Completed
• Phase: N/A
• First received: January 3, 2013
• Last updated: January 7, 2013
• Start date: October 2010
• Est. completion date: March 2011

Study information

• Verified date: January 2013
• Source: Yonsei University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Korea: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

Recently epiaortic ultrasound scanning (EAS) has been recommended as an intraoperative tool to accurately assess ascending aorta disease. To date, several studies have reported that EAS is superior to TEE and surgical palpation

Recruitment information / eligibility

• Status: Completed
• Enrollment: 2292
• Est. completion date: March 2011
• Est. primary completion date: March 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 31 Years to 88 Years

Eligibility

Inclusion Criteria:

patients underwent who isolated off-pump coronary artery bypass

Exclusion Criteria:

1. combined carotid procedures

2. preoperative cerebral haemorrhage

3. nonoperative unstable vital signs such as ventricular fibrillation or cardiac arrest

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Coronary Artery Occlusive Disease

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Yonsei University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Early Stroke After Off-pump Coronary Artery Bypass		number of incidence of early strok from surgery to discharge, an expected average of 5 weeks	No