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NCT01410318Active, not recruiting

Progression of Early Subclinical Atherosclerosis

Early Detection and Progression of Subclinical Atherosclerosis and Its Relationship to Coronary Risk Factors

Source: ClinicalTrials.gov · Last updated 29 Apr 2021

Brief summary (registry, in English)

The overall objective of this study is to characterize the prevalence and progression rate of subclinical atherosclerotic lesions and to study their association to the imaging characteristics of atheroma plaques and to the presence of genetic, epigenetic, metabolomic, and environmental factors, including dietary habits, physical activity, biorhythms, psychosocial characteristics, and exposure to environmental pollutants

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
4184 (actual)
First submitted
2 Aug 2011
Start date
14 Jun 2010
Primary completion date
30 Jun 2030
Lead sponsor
Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III
NCT number
NCT01410318

What you commit to

  • Study type: Observational
  • Participants enrolled: 4184
  • From 14 Jun 2010 to the primary completion date, 30 Jun 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior angioplasty or heart surgery
  • A chest CT in the previous year

Other illness

  • Myocardial Infarction
  • Angina pectoris
  • Stroke, either transient or with sequelae
  • Peripheral vascular disease
  • Other heart diseases
    • Subjects with the following conditions will also be excluded:
  • Active treatment for any cancer

Lab values

  • Renal failure with creatinine clearance \<60 mL/min, as estimated by the Cockcroft and Gault formula

Age

  • Any disease that decreases life expectation to ≤6 years

Other

  • Atrial fibrillation
  • Pregnancy
  • Morbid obesity (BMI ≥40)
  • Pacemaker, implantable automatic defibrillator, or any implanted device that contraindicates MRI

Who the study is looking for

  • Employees of the Banco de Santander Group
  • Age between 40-54 years.

Age in the registry: 40 years to 54 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ciudad Financiera del Grupo Santander
Coordinator of this site? Confirm its status
Boadilla del MonteSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.