"Preventing Cardiovascular Ischemic Events and Arresting Their Consequences in Type 2 Diabetic Population
NCT ID: NCT02248311
Last Updated: 2018-01-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
260 participants
OBSERVATIONAL
2014-09-30
2018-10-31
Brief Summary
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A prolonged sub-clinical phase exists before a Cardiovascular event occurs in Type 2 Diabetes patients. Therefore, new strategies aimed at identifying those patients with this subclinical Cardiovascular Diabetes and, consequently, more prone to develop Cardiovascular events is a challenge to be met.
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Detailed Description
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1\) To examine whether the extension and degree of microangiopathy is an independent risk factor for silent myocardial and brain ischemia. 2) To evaluate whether the degree and extension of microangiopathy is a predictor of CV events and poor outcome. 3) To evaluate whether a new score based on the extension and the degree of microangiopathy will permit us to improve the current methods used to identify patients at risk of CVD and its outcomes. 4) To determine whether the presence and the degree of NAFLD is an independent Cardiovascular disease risk factor and represent and extra-value to the score based on the extension and the degree of microangiopathy.
Secondary objectives:
1\) To examine the usefulness of selected serum biomarkers in identifying diabetic patients at risk of Cardiovascular disease 2) To evaluate whether these selected biomarkers are related to the degree and extension of microangiopathy and the outcome of cardiovascular events. 3) To better define the meaning of microalbuminuria in type 2 diabetic population (glomerular involvement vs. index of generalized endothelial dysfunction)
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Patients/Control Group
Observational
No interventions assigned to this group
Patients/Group Control
Observational
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
50 Years
79 Years
ALL
Yes
Sponsors
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Hospital Universitari Vall d'Hebron Research Institute
OTHER
Responsible Party
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Principal Investigators
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David García-Dorado Garcia, PhD MD
Role: PRINCIPAL_INVESTIGATOR
Hospital Universitario Valle de Hebron, Barcelona, Spain
Joan Montaner Vilallonga, PhD MD
Role: PRINCIPAL_INVESTIGATOR
Hospital Universitario Valle de Hebron, Barcelona, Spain
Rafael Simó Canonge, PhD MD
Role: PRINCIPAL_INVESTIGATOR
Hospital Universitario Valle de Hebron, Barcelona, Spain
Joan Sayós Ortega, PhD MD
Role: PRINCIPAL_INVESTIGATOR
Hospital Universitario Valle de Hebron, Barcelona, Spain
Daniel Serón Micas, PhD MD
Role: PRINCIPAL_INVESTIGATOR
Hospital Universitario Valle de Hebron, Barcelona, Spain
Joan Genescà Ferrer, PhD MD
Role: PRINCIPAL_INVESTIGATOR
Hospital Universitario Valle de Hebron, Barcelona, Spain
Santiago Aguadé Bruix, PhD MD
Role: PRINCIPAL_INVESTIGATOR
Hospital Universitario Valle de Hebron, Barcelona, Spain
Joan Xavier Comella Carnicé, PhD MD
Role: PRINCIPAL_INVESTIGATOR
Hospital Universitario Valle de Hebron, Barcelona, Spain
Locations
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Hospital Universitario Valle de Hebron
Barcelona, , Spain
Countries
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Other Identifiers
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PRECISED ISCiii-PIE-13
Identifier Type: -
Identifier Source: org_study_id
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