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TerminatedNCT00982852Updated Jul 12, 2013

Intravascular Ultrasound Derived Virtual Histology and Intracoronary Serum Markers of Inflammation

An observational study in Coronary Artery Disease, Atherosclerosis and Myocardial Infarction, sponsored by Quinn Capers. Terminated at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-07-12.

Sponsored by Quinn Capers · Observational

Why this study was terminated
Lack of funding
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
9
Ages
18 Years and older
Sex
All
01

Study summary

Patients enrolled will need treated with an IVUS- VH (intravascular ultrasound-derived virtual histology) which is an arterial stent procedure, that involves threading a tiny wire into the artery, followed by a balloon, a stent, or other device to treat a blocked artery, and often (though not always), a special ultrasound catheter to take pictures of the inside of the artery.

Participants in the study, will have an additional procedure performed: a tiny tube will be advanced into the heart artery to collect a blood sample for research purposes, and a blood sample will be collected from the femoral (thigh) artery through the tube that will be placed there as a standard part of having this procedure.

The blood that is collected will be analyzed for markers of inflammation or irritation in the blood (c-reactive protein, myeloperoxidase, Monocyte chemotactic protein-1), as well and a gene called Matrix Metallopeptidase 3, which is believe to influence the progression of plaque on the walls of arteries and the progression of coronary artery disease. .

Read the detailed description

Patients that have severe blockage in one of the arteries that provides blood flow to your heart will be enrolled into the research study. Most of the procedures in the study standard care used by cardiologists when treating blocked arteries. Patients enrolled will need treated with an IVUS- VH (intravascular ultrasound-derived virtual histology) which is an arterial stent procedure, that involves threading a tiny wire into the artery, followed by a balloon, a stent, or other device to treat a blocked artery, and often (though not always), a special ultrasound catheter to take pictures of the inside of the artery. We will collect all the data from the above stated standard medical care procedure.

Participants in the study, will have an additional procedure performed: a tiny tube will be advanced into the heart artery to collect a blood sample for research purposes, and a blood sample will be collected from the femoral (thigh) artery through the tube that will be placed there as a standard part of having this procedure.

The blood that is collected will be analyzed for markers of inflammation or irritation in the blood (c-reactive protein, myeloperoxidase, Monocyte chemotactic protein-1), as well and a gene called Matrix Metallopeptidase 3, which is believe to influence the progression of plaque on the walls of arteries and the progression of coronary artery disease. .

Finally, after discharged from the hospital, the research nurses will call you at home to ask you questions about how you are doing for approximately 5-10 minutes. Telephone follow-up will occur at one month, six months, 12 months, 18 months, 24 months, and 36 months.

02

Conditions studied

  • Coronary Artery Disease
  • Atherosclerosis
  • Myocardial Infarction
  • Heart Failure
  • Angina

Keywords

  • Angioplasty
  • Coronary Vessels
  • Heart Disease
  • Cardiology
  • Atherosclerosis
  • Catheterization
03

In context

Coronary Artery Disease

5,598 studies on the registry are indexed under Coronary Artery Disease; 957 are open to participants now.

This study's enrollment of 9 is below the median of 336 across 1,947 observational studies indexed under Coronary Artery Disease.

Browse Coronary Artery Disease studies →

Lead sponsor

This is the only study on the registry with Quinn Capers as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients in need of angioplasty or left heart catheterization

Inclusion criteria

  • In- or out-patients admitted to IPR or hospital floor for left heart catheterization or scheduled angioplasty
  • 18 years or older
  • Able to provide informed consent

Exclusion criteria

Exclusion Criteria:

  • Patients who are pregnant or lactating
  • Inability to provide informed consent
  • Patients undergoing heart catheterization for who open heart surgery is planned
  • Anticipate being unavailable for telephone follow-up
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
9 participants (actual)
Biospecimen retention
Samples with dna

Groups and cohorts

  • Acute

    Patients in acute need for angioplasty or left heart catheterization.

  • Chronic or non-acute

    Patients will planned angioplasty or left heart catheterization.

06

What researchers measure

Primary outcomes

  1. Occurrence or absence of adverse cardiovascular outcomes up to 36 months after PCI

    Time frame: 36 months

07

Study locations

1 site
  • The Ohio State University Medical Center
    Columbus, Ohio 43210, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 12, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00982852
Lead sponsor
Quinn Capers
Responsible party
Quinn Capers (Professor, Ohio State University) — Sponsor-investigator
First posted
Sep 23, 2009
Start date
Dec 2008
Primary completion
Jul 2009
Completion
Dec 2010
Last update
Jul 12, 2013

Study contacts

Quinn Capers IV, MD
principal investigator · Ohio State University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jul 2013. You cannot join it, but the record below documents what was studied.

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