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Clinical Trials/NCT00580580
NCT00580580
Withdrawn
Not Applicable

The Detection of Coronary Stenosis With Intravenous Mircrobubbles and Contrast Pulse Sequence Low Mechanical Index Imaging

University of Nebraska0 sitesFebruary 2012

Overview

Phase
Not Applicable
Intervention
Optison
Conditions
Coronary Stenosis
Sponsor
University of Nebraska
Primary Endpoint
Detection of coronary and carotid artery stenoses and perfusion defects during standard echocardiographic examination
Status
Withdrawn
Last Updated
2 years ago

Overview

Brief Summary

To detect coronary artery disease by both coronary and carotid artery imaging and myocardial perfusion imaging using a new low mechanical index real time system.

Detailed Description

The objective of this clinical study will be to visualize both coronary and carotid arteries as well as detect myocardial perfusion following a routine intravenous injection of Definity (0.05-0.20 millimeters), Optison (0.1-0.4 millimeters) or PESDA (0.05-0.2 mL). Following these injections , we will attempt to Contrast Pulse Sequencing on the Siemens Acuson Sequoia system to image both the coronary and carotid arteries, as well as the Myocardial perfusion.

Registry
clinicaltrials.gov
Start Date
February 2012
End Date
March 2014
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • subjects scheduled for routine echocardiogram to look for evidence of Coronary artery disease or a stress echocardiogram
  • women of child-bearing potential must be taking a medically approved form of birth control with a negative urine pregnancy test
  • be conscious and coherent, and be able to communicate effectively with study personnel
  • last eight patients will be diabetics who smoke
  • provide informed consent after receiving a verbal and written explanation of the purpose and nature of the study

Exclusion Criteria

  • severe valvular heart disease by Doppler Echocardiography
  • females of child-bearing potential who are not taking a medically approved method of birth control will be excluded. If the patient is pregnant she will be excluded.
  • patients who are allergic to blood or blood products will be excluded
  • have contraindication to Optison, Definity, or PESDA (pulmonary HTN, cardiac shunt)
  • non diabetics, non smokers

Arms & Interventions

1 Intravenous Optison Followed by Contrast Pulse Sequencing

Administration of Optison (0.1-0.4 mL) intravenously followed by Contrast Pulse Sequencing to image both the coronary and carotid arteries. Use will depend on availability of the contrast for the given study Optison will not be used on patients with blood allergies or Jehovah Witnesses

Intervention: Optison

2 Intravenous Definity followed by Contrast Pulse Sequencing

Intravenous injection of Definity (0.05-0.20 mL) followed by Contrast Pulse Sequencing to image both coronary and carotid arteries

Intervention: Definity

3 Intravenous PESDA followed by Contrast Pulse Sequencing

Intravenous injection of PESDA at a rate of 0.05-0.20 mL followed by Contrast Pulse Sequencing image of coronary and carotid arteries PESDA will be used exclusively in patients who are eligible for other IRB studies

Intervention: PESDA

Outcomes

Primary Outcomes

Detection of coronary and carotid artery stenoses and perfusion defects during standard echocardiographic examination

Time Frame: 2-4 months

To determine whether this imaging scheme can detect both coronary and carotid artery stenoses as well as perfusion defects during a standard echocardiographic examination

Secondary Outcomes

  • Visual analysis of coronary and carotid arteries and perfusion defects during standard echocardiogram examination(immediate)

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