Longitudinal Strain in Addition to Visual Assessment of Wall Motion for Ruling in Ischemia in the Emergency Room

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2010 by Hillel Yaffe Medical Center.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Hillel Yaffe Medical Center
ClinicalTrials.gov Identifier:
NCT01111643
First received: April 25, 2010
Last updated: April 26, 2010
Last verified: April 2010
  Purpose

To assess the utility of technician-based analysis of echocardiograms with longitudinal strain for ruling-in ischemic chest pain in the emergency room, compared to emergency room (ER) physician opinion and expert echocardiographer analysis of wall motion, both the latter blinded to any relevant clinical data .


Condition Intervention
Chest Pain
Device: Echocardiogram

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by Hillel Yaffe Medical Center:

Estimated Enrollment: 500
Study Start Date: April 2008
Estimated Study Completion Date: May 2011
Estimated Primary Completion Date: May 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
I Device: Echocardiogram
An echocardiogram will be repeated at every step, from baseline to peak heart rate setting.

  Eligibility

Ages Eligible for Study:   20 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients admitted to the ER because of chest pain with no prior history coronary artery disease.

Criteria

Inclusion Criteria:

  • Chest pain
  • No indication of acute myocardial infarction

Exclusion Criteria:

  • Patients admitted for acute myocardial infarction
  • Patients with known coronary artery disease
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01111643

Locations
Israel
Emergency Department Hille Yaffe Medical Center Recruiting
Hadera, Israel, 38100
Contact: David S Blondheim, MD    972-4630-4488    davidb@hy.health.gov.il   
Principal Investigator: David S. Blondheim, MD         
Sponsors and Collaborators
Hillel Yaffe Medical Center
  More Information

No publications provided

Responsible Party: David S. Blondheim, MD, Hillel Yaffe Medical Center
ClinicalTrials.gov Identifier: NCT01111643     History of Changes
Other Study ID Numbers: 0023-08-HYMC-CTIL
Study First Received: April 25, 2010
Last Updated: April 26, 2010
Health Authority: Israel: Ministry of Health

Additional relevant MeSH terms:
Chest Pain
Pain
Signs and Symptoms

ClinicalTrials.gov processed this record on September 16, 2014