NCT01122069

Brief Summary

In patients with acute myocardial infarction, treatment logistics are primarily defined based upon ST segment shift in the electrocardiogram. While patients with ST elevation (STEMI) are forwarded to immediate coronary angiography and percutaneous coronary intervention, patients without ST elevation (NSTEMI) are initially medically treated and recommended coronary angiography within 48-72 hours. Early invasive treatment has been found cost-effective in intermediate and high-risk NSTEMI patients and current guidelines recommend use of the Thrombolysis in Myocardial Infarction (TIMI) risk score to identify patients who will benefit from early intervention due to high risk of new infraction and cardiovascular death. However, new research has suggested that TIMI risk score may not always identify patients with severe angiographic disease. The purpose of this study was to assess if contrast echocardiography could be used to identify NSTEMI patients with angiographically severe disease independent of their TIMI risk score.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
110

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2008

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2008

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2009

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

May 10, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 12, 2010

Completed
Last Updated

June 15, 2025

Status Verified

June 1, 2025

Enrollment Period

1.3 years

First QC Date

May 10, 2010

Last Update Submit

June 11, 2025

Conditions

Study Arms (1)

Contrast echocardiography

110 patients with acute non-ST elevation myocardial infarct were examined with contrast echocardiography prior to coronary angiography.

Other: Perflutren Lipid Microsphere ultrasound contrast

Interventions

Perflutren Lipid Microsphere ultrasound contrast 0.01 ml/kg administered as intravenous bolus

Also known as: Luminity
Contrast echocardiography

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

110 patients with acute non-ST elevation myocardial infarction

You may qualify if:

  • acute non-ST elevation myocardial infarction

You may not qualify if:

  • hemodynamic unstable
  • mechanical prosthetic heart valve
  • severly reduced pulmonary function

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Heart Disease, Haukeland University Hospital

Bergen, Norway

Location

Related Publications (2)

  • Eskerud I, Gerdts E, Nordrehaug JE, Lonnebakken MT. Global Coronary Artery Plaque Area is Associated with Myocardial Hypoperfusion in Women with Non-ST Elevation Myocardial Infarction. J Womens Health (Larchmt). 2015 May;24(5):367-73. doi: 10.1089/jwh.2014.4920. Epub 2015 Feb 18.

  • Lonnebakken MT, Nordrehaug JE, Gerdts E. No gender difference in the extent of myocardial ischemia in non-ST elevation myocardial infarction. Eur J Prev Cardiol. 2014 Jan;21(1):123-9. doi: 10.1177/2047487312454107. Epub 2012 Jul 2.

MeSH Terms

Conditions

Non-ST Elevated Myocardial Infarction

Interventions

perflutren

Condition Hierarchy (Ancestors)

Myocardial InfarctionMyocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosis

Study Officials

  • Mai Tone Lønnebakken, MD

    University of Bergen, Bergen, Norway

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Cardiology

Study Record Dates

First Submitted

May 10, 2010

First Posted

May 12, 2010

Study Start

March 1, 2008

Primary Completion

July 1, 2009

Study Completion

July 1, 2009

Last Updated

June 15, 2025

Record last verified: 2025-06

Locations