"Preventing Cardiovascular Ischemic Events and Arresting Their Consequences in Type 2 Diabetic Population

NCT ID: NCT02248311

Last Updated: 2018-01-23

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

260 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-09-30

Study Completion Date

2018-10-31

Brief Summary

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Current methods based on traditional Cardiovascular risk factors are not clinically useful for identifying Type 2 Diabetes patients at risk of developing acute Cardiovascular ischemic events (ie.myocardial infarction or stroke). In addition, Cardiovascular ischemic events in Type 2 Diabetes population have worse prognosis than in general population. In fact, there is sufficient experimental evidence indicating that diabetes exaggerates the deleterious effects of ischemic events and worsens their outcome.

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.

Detailed Description

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Objectives

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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Type2 Diabetes Mellitus Microangiopathy Non Alcoholic Fatty Liver Disease Coronary Artery Disease Cerebrovascular Disease Acute Coronary Syndrome/ Myocardial Infarction Ictus

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

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

* a) Age from 50-79 years; b) History of type 2diabetes of at least one year. Diabetes will be defined following the American Diabetic Association criteria: fasting glucose level of at least 126 mg/dl \[7.0 mmol/l\] in two separate analyses, a non-fasting glucose level of at least 200 mg/dl \[11.1 mmol/l\] or a self-reported history of physician-diagnosed diabetes or treatment for diabetes

Exclusion Criteria

* a) Past medical history of Cardiovascular event; b) Type 1 diabetes; c) Contraindication for PET-CT or MRI d) Other concomitant disease associated with a short life expectancy
Minimum Eligible Age

50 Years

Maximum Eligible Age

79 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hospital Universitari Vall d'Hebron Research Institute

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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Spain

Other Identifiers

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PRECISED ISCiii-PIE-13

Identifier Type: -

Identifier Source: org_study_id

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