Biological Phosphocalcic Metabolism and Coronary Artery Calcifications

NCT ID: NCT02792868

Last Updated: 2017-04-07

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

COMPLETED

Total Enrollment

83 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-04-30

Study Completion Date

2017-03-31

Brief Summary

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Study a sample of patients in primary prevention, moderate cardiovascular risk (n = 83 patients), with normal, non-diabetic renal function. The investigators quantify the phophocalcic intake and excretion, realizing a food examination and a urine collection of 24 particular. The investigators will measure plasma levels of FGF23 serum calcium, phosphatemia, the investigators will calculate the tubular reabsorption of phosphate. The investigators will conduct a quantitative assessment of coronary calcification by a non-injected CT scan, measuring semi automated way Agatston calcium score. There will be an analysis of collinearity. An adjustment will be made for confounding variables in a generalized linear regression model.

Detailed Description

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Conditions

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Cardiovascular Disease

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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patient

patient with cardiovascular risk (moderate)

24 h urines analyses

Intervention Type OTHER

patient collects urines during 24h

Interventions

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24 h urines analyses

patient collects urines during 24h

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Hospitalization for a cardiovascular check in the Detection Centre and the Atherosclerosis Prevention (CHU Rangueil Toulouse)
* In primary prevention of coronary heart disease
* Introducing an intermediate cardiovascular risk according to the European SCORE equation, that is to say, a risk of cardiovascular death at 10 years greater than or equal to 1% and less than 5%
* signed the informed consent,

Exclusion Criteria

* Chronic renal failure patients with an estimated GFR less than 60 mL / min / 1.73m2, due to alterations in phosphate metabolism,
* Patients receiving glucose-lowering therapy,
* Patients with a fasting blood glucose greater capillary or equal to 1.10 g / l, confirmed by a plasma glucose greater than or equal to 1.10g / l.
* The diuretic therapy patients (due to a change in urinary electrolytes)
* HIV-positive patients for HIV, antiretroviral (due to a change in urinary electrolytes)
* Pregnant women,
* Patients under judicial protection, guardianship or trusteeship.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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French Cardiology Society

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jean FERRIERES

Role: PRINCIPAL_INVESTIGATOR

CHU RANGUEIL

Locations

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Chu Rangueil

Toulouse, , France

Site Status

Countries

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France

Other Identifiers

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2015.02

Identifier Type: -

Identifier Source: org_study_id

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