Detection no Invasive of a Silent Myocardial Ischemia

NCT ID: NCT02885428

Last Updated: 2022-10-13

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

TERMINATED

Total Enrollment

47 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-04-15

Study Completion Date

2018-04-17

Brief Summary

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The pathophysiological features of myocardial diabetic subject combined with cardiac autonomic neuropathy were behind the quietness of myocardial ischemia, known as silent myocardial ischemia (IMS). These patients have the risk to remain asymptomatic until the sudden onset of a myocardial infarction, or even sudden death.

That is why the investigators want to evaluate the contribution of non-invasive tools to stand in the diagnosis of IMS patients with diabetes type 2, asymptomatic heart on map: Technical myocardial speckle tracking in studying strains overall average left ventricular (longitudinal, circumferential and radial) measured in 2D and 3D at rest, compared to stress echocardiography with dobutamine (ESD)

Detailed Description

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Conditions

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Silent Myocardial Ischemia Type 2 Diabetes

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Interventions

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echography

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* With at least two cardiovascular risk factors including: hypertension, dyslipidemia, smoking active or interrupted for less than 3 years, family history (relatives of the 1st degree) Accident major CV before 60.
* Or whatever the level of risk factors: peripheral artery disease and / or carotid atherosclerosis, or proteinuria

Exclusion Criteria

* Valvular heart disease (severe to moderate valvular ) , hypertrophic , dilated , chronic lung
* History of cardiotoxic chemotherapy
* Atrioventricular blocks of degree
* Asthma
* Recent stroke within a month
* Bilateral carotid stenosis tight
* Glaucoma untreated narrow angle
* Subject to exclusion period (determined by a previous study or in progress)
* Inability to give informed about information
* patient under judicial protection
* patient guardianship or curatorship
* Current pregnancy (women of childbearing age )
* Breastfeeding
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Strasbourg, France

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Samy TALHA, MD

Role: PRINCIPAL_INVESTIGATOR

Hôpitaux Universitaires de Strasbourg

Locations

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Les Hôpitaux Universitaires

Strasbourg, , France

Site Status

Countries

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France

Other Identifiers

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2014-A01458-39

Identifier Type: -

Identifier Source: org_study_id

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