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NCT01236313 Clinical Trial

Aortic Wall and Left Ventricular Mechanics: Echocardiographic and Hemodynamic Analysis

Coronary Disease Clinical Trial

Official title:
Aortic Wall and Left Ventricular Mechanics: Echocardiographic and Hemodynamic Analysis

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT01236313
Other study ID # 1005011039
Secondary ID
Status Terminated
Phase N/A
First received November 4, 2010
Last updated February 16, 2016
Start date July 2010
Est. completion date March 2014

Study information
Verified date February 2016
Source Weill Medical College of Cornell University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to prospectively determine the relationship between the dimensions of the aorta (the large artery taking off the heart) and blood pressure during cardiac surgery.

Description:

The purpose of this study is to prospectively determine the relationship between the dimensions of the aorta (the large artery taking off the heart) and blood pressure during cardiac surgery. Measurements of the aorta are obtained by an ultrasound-based imaging technique called transesophageal echocardiography (TEE), which is routinely performed during cardiac surgery. TEE is an instrument used to monitor the heart and is standard of practice at Weill Cornell Medical College.

Recruitment information / eligibility
Status Terminated
Enrollment 51
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- elective CABG, valvular procedure

Exclusion Criteria:

- non-sinus rhythm (atrial fibrillation, flutter, paced rhythm), pre-operative presence of intra-aortic counterpulsation device, synthetic aortic graft.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Procedure:
• TEE report
Information will be collected during cardiac surgery.

Locations
Country Name City State
United States Weill Cornell Medical College New York New York

Sponsors (1)
Lead Sponsor Collaborator
Weill Medical College of Cornell University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Measure the dimensions of the aorta and compare with blood pressure measurements 1 No
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