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Correlation of Artherosclerotic Plaque Volume and Intima Media Thickness With Soluble P-selectin

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ClinicalTrials.gov Identifier: NCT01895725
Recruitment Status : Recruiting
First Posted : July 10, 2013
Last Update Posted : September 28, 2017
Sponsor:
Information provided by (Responsible Party):
Peter Marschang, Medical University Innsbruck

Brief Summary:
The proposed project is a prospective observational, single-center cohort study aimed to examine the progression of atherosclerotic alterations of the carotid arteries (IMT, plaque volume) during a follow-up of up to four years and to correlate the observed changes with traditional and novel biomarkers of atherosclerosis. A total of 600 subsequent patients with or established cardiovascular disease or at least one cardiovascular risk will be tested with a high-frequency ultrasound probe equipped with automated IMT measurements and 3D quantitative plaque volumetry. Plasma samples will be collected and tested for traditional and novel cardiovascular risk factors. Both ultrasound examinations and blood sampling will be repeated once per year to assess changes in these parameters over time depending on treatment modalities, which are left to the discretion of the treating physicians. The primary endpoint of the planned study will be the correlation between P-selectin and the progression of atherosclerosis as measured by plaque volume and IMT in the carotid and femoral arteries, respectively. Secondary endpoints will include the correlation of established (hypertension, smoking, diabetes, dyslipidemia) and novel risk factors (hsCRP, P-selectin, cholesteryl ester transfer protein (CETP), intercellular adhesion molecule-1 (ICAM-1), CETP TaqIb polymorphism) with the progression of atherosclerosis, the correlation of cardiovascular events with the progression of atherosclerosis and the additional predictive value of plaque volume and IMT compared to an established risk score (SCORE card).

Condition or disease
Cardiovascular Risk Factors Coronary Artery Disease Cerebrovascular Disease Peripheral Artery Disease

Study Type : Observational
Estimated Enrollment : 600 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Correlation of Artherosclerotic Plaque Volume and Intima Media Thickness With Soluble P-selectin
Study Start Date : June 2013
Estimated Primary Completion Date : June 2019
Estimated Study Completion Date : June 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Atherosclerosis
U.S. FDA Resources




Primary Outcome Measures :
  1. Correlation between P-selectin and the progression of atherosclerosis [ Time Frame: up to 4 years ]
    The primary endpoint of the planned study will be the correlation between P-selectin and the progression of atherosclerosis as measured by plaque volume and IMT in the carotid and femoral arteries


Secondary Outcome Measures :
  1. Correlation of cardiovascular events with the progression of atherosclerosis [ Time Frame: up to 4 years ]
    As secondary endpoints, cardiovascular events (cardiovascular death, myocardial infarction, percutaneous transluminal coronary angioplasty (PTCA), coronary bypass surgery, stroke, transient ischemic attack (TIA), surgery for aortic aneurysm, critical limb ischemia, peripheral percutaneous transluminal angioplasty (PTA), peripheral bypass) will be correlated with the progression of atherosclerosis and the additional predictive value of plaque volume and IMT in carotid and or femoral arteries compared to an established clinical risk score risk score (SCORE card) will be calculated


Biospecimen Retention:   Samples With DNA
Plasma samples


Information from the National Library of Medicine

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Ages Eligible for Study:   30 Years to 85 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients referred to ultrasound examinations of the carotid and/or femoral arteries for standard indications will be screened for potential inclusion into the study
Criteria

Inclusion Criteria:

  • Patients (male and female) aged 30 to 85 years
  • with at least one traditional cardiovascular risk factor (hypertension, smoking, diabetes, dyslipidemia, family history) or established coronary artery disease, cerebrovascular disease, or peripheral artery disease diagnosed by objective testing

Exclusion Criteria:

  • lack of informed consent
  • the impossibility of follow-up testing once per year for the following four years

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01895725


Contacts
Contact: Peter Marschang, MD +43-512-504-81414 peter.marschang@i-med.ac.at

Locations
Austria
Medical University Innsbruck, Department for Internal Medicine III Recruiting
Innsbruck, Austria, 6020
Contact: Peter Marschang, MD       peter.marschang@i-med.ac.at   
Principal Investigator: Peter Marschang, MD         
Sponsors and Collaborators
Medical University Innsbruck
Investigators
Principal Investigator: Peter Marschang, MD Medical University Innsbruck

Responsible Party: Peter Marschang, Prof. MD, Medical University Innsbruck
ClinicalTrials.gov Identifier: NCT01895725     History of Changes
Other Study ID Numbers: P-selectin 03-13
First Posted: July 10, 2013    Key Record Dates
Last Update Posted: September 28, 2017
Last Verified: September 2017

Additional relevant MeSH terms:
Cerebrovascular Disorders
Coronary Artery Disease
Myocardial Ischemia
Coronary Disease
Peripheral Arterial Disease
Heart Diseases
Cardiovascular Diseases
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases
Atherosclerosis
Peripheral Vascular Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases