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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01515267
Other study ID # DIA100
Secondary ID
Status Active, not recruiting
Phase N/A
First received January 18, 2012
Last updated January 23, 2012
Start date November 2011

Study information

Verified date January 2012
Source Diacardio LTD
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Left ventricular ejection fraction (EF) is evaluated in every echocardiographic examination either by visual estimation (eyeballing) requiring high level of training and expertise and/or by manual tracing of the endocard from which EF is calculated (manual biplane method (MBP)). This procedure is subjective and time consuming. The objective of this study is to compare the performance of LVivoEF software system to the measurements obtained by the routinely used methods.


Description:

LVivoEF is a decision support system (software) for automated global left ventricle (LV) systolic function evaluation from echocardiographic examinations. LVivoEF technology is based on a novel image processing algorithm for LV edge detection and ejection fraction (EF) evaluation. LVivoEF provides fully automated measurements of the left ventricle (LV) from two apical views the four chamber (4CH) and the two chamber (2CH).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 100
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age > 18

- Patients referred to an echocardiographic examination. The patients will be consecutive until 30% of patients with normal LV function are enrolled. After that only consecutive patients with abnormal LV function will be included.

Exclusion Criteria:

- Examinations in which more than one third of the endocard is not visible in a plane (2CH/4CH)

- Patients with Left bundle branch block (LBBB)

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Soroka university medical center Beer-Sheva

Sponsors (1)

Lead Sponsor Collaborator
Diacardio LTD

Country where clinical trial is conducted

Israel, 

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