Home
Clinical Trials
Intraoperative Epiaortic Scan...

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

Last Updated: 2013-01-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

2292 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-10-31

Study Completion Date

2011-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Relationship Between a Combined Index of Diastolic and Systolic Performance and Intraoperative Hemodynamic Changes During Off-pump Coronary Bypass Surgery

NCT02534103

Coronary Artery Obstructive Disease

COMPLETED

Transesophageal Echocardiography (TEE) and Simulation : a Preferred Learning Path

NCT06164171

Cardiac Disease

RECRUITING

Intraoperative Transesophageal Echocardiography Assessment of Portal Vein Flow and Renal Resistive Index As a Predictor of Acute Kidney Injury After Cardiac Surgery: A Prospective Observational Study

NCT04112953

AKI

COMPLETED

Influence of Lung Ultrasonography on the Prognosis and Postoperative Outcomes in Cardiac Surgical Patients

NCT06377449

Ischemic Heart Disease Aortic Stenosis, Severe Aortic Insufficiency +5 more

RECRUITING NA

3D & Speckle Tracking Together as a Marker for Early Outcome in Cardiac Surgery

NCT02642770

Left Ventricular Systolic Dysfunction

COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Coronary Artery Occlusive Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

non epiaortic group

non epiaortic group ( n=1019)

No interventions assigned to this group

epiaortic group

epiaortic group ( n=1273)

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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

Minimum Eligible Age

31 Years

Maximum Eligible Age

88 Years

Eligible Sex

ALL

Accepts Healthy Volunteers