NESCAV Nutrition Environment and Cardiovascular Health

The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2010 by Central Hospital, Nancy, France.
Recruitment status was  Recruiting
Sponsor:
Collaborators:
CIC-P
FEDER
CRP-Santé Luxembourg
ULG Wallonie
Information provided by:
Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT01414179
First received: August 10, 2011
Last updated: NA
Last verified: August 2010
History: No changes posted
  Purpose

Introduction. The cardiovascular diseases, at the origin of 4 deaths out of 10, remain the leading cause of mortality in Europe. According to WHO, this tendency will spread in 2020 on a worldwide scale. These pathologies are avoidable on the whole by the adoption of healthy lifestyles. To prevent occurred of the cardiovascular affections is, more than ever, a major goal of Public health. The transborder "Great Area", localised zone in the middle of Europe between the very high cardiovascular risks of the North and the weaker risks of the South, constitutes a zone privileged for the action against the cardiovascular diseases. However, there to date does not exist any joint action in this geographical area. The Public Research centre of the Health of the Grand-Duchy of Luxembourg, the School of Public health of the University of Liege, the Clinical Center of Investigation of the University hospital of Nancy and the University hospital of the Saar wish to be linked and mutualiser their means available and their complementary competences in order to evaluate and to act on the cardiovascular health of the citizens of the "Great Area". Over one 3 years period the Nutrition project, Environment and Cardiovascular Health (NESCAV) aims at creating on the level of the Great Area a transborder alliance of prevention and promotion of cardiovascular health. This great multicentric transverse investigation and poly-set of themes will make it possible to collect relevant data on cardiovascular health of the population of the Great area.

Objective of this biomedical research project: It is about multicentric, transverse a Européenne epidemiological study aiming, through biological questionnaires and analyses, to collect information on the cardiovascular risk factors within the Great Area.


Condition
Cardiovascular Pathology

Study Type: Observational
Study Design: Observational Model: Ecologic or Community
Time Perspective: Prospective
Official Title: Nutrition Environnement et Santé Cardio Vasculaire NESCAV

Further study details as provided by Central Hospital, Nancy, France:

Biospecimen Retention:   Samples Without DNA

Blood and urinary biological taking away: glycemia, HbA1C, insulin (specific study analyzes), total cholesterol, HDL cholesterol, LDL cholesterol, triglycerides, apolipoproteines A1 and B, numeration of blood picture, creatinin, uric acid, gamma WP, GOT, GPT, CRP; and a urinary collection (a micturition) in order to proportion the microalbuminurie. A plasmathèque will be made up, in order to measure later on biomarqueurs of the cardiovascular risk (biological collection stored with the CIC). A measurement of pollutants and poisons will be carried out starting from taking away of hair.


Estimated Enrollment: 800
Study Start Date: October 2010
Estimated Study Completion Date: December 2011
Estimated Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Detailed Description:

Methods: In Lorraine, this study will be carried out on 800 subjects from 18 to 69 years taking part simultaneously in a quinquennial assessment of preventive medicine (CPAM), in the Centers of Preventive medicine (CMP) of Nancy and Longwy. The study will proceed on 1 year and six months, the recruitment of the volunteers will finish with the end of the year 2011. Data collected: General questionnaire, medical examination Quantification of the nutritional contributions Perception of the participant on the methods of assumption of responsibility of various risk factors cardiovascular Blood and urinary biological taking away: glycemia, HbA1C, insulin (specific study analyzes), total cholesterol, HDL cholesterol, LDL cholesterol, triglycerides, apolipoproteines A1 and B, numeration of blood picture, creatinin, uric acid, gamma WP, GOT, GPT, CRP; and a urinary collection (a micturition) in order to proportion the microalbuminurie. A plasmathèque will be made up, in order to measure later on biomarqueurs of the cardiovascular risk (biological collection stored with the CIC). A measurement of pollutants and poisons will be carried out starting from taking away of hair. (analyzes realized in Luxembourg) Data analysis: All the relative data with the participants will be anonymisées with the CMP before export to the CIC. These anonymized data will also be the subject of a treatment computerized in the countries taking part in the study, and a database common to the partners of the Great area will be made up, in order to compare the characteristics of the 3 transborder populations.

  Eligibility

Ages Eligible for Study:   18 Years to 69 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

general population

Criteria

Inclusion Criteria:

  • men or women aged 18 till 69 years old
  • living in Lorraine since 5 years
  • speaking and understanding French language
  • having signed the assent
  • Having a social security number

Exclusion Criteria:

  • taking part of the study refusal
  • signature assent refusal
  • pregancy
  • minor people
  • People under supervision or under trusteeship
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01414179

Contacts
Contact: Celine Hertz +33 3 83 15 73 12 cel.hertz@chu-nancy.fr

Locations
France
Centre médecine Preventive Recruiting
Vandoeuvre lès Nancy, France, 54500
Contact: Celine Hertz    +33 3 83 15 73 12    cel.hertz@chu-nancy.fr   
Sponsors and Collaborators
Central Hospital, Nancy, France
CIC-P
FEDER
CRP-Santé Luxembourg
ULG Wallonie
Investigators
Principal Investigator: Faiez ZANNAD, PU-PH CIC-P
  More Information

No publications provided

Responsible Party: Pr. Faiez ZANNAD, CIC-P, CHU de Nancy
ClinicalTrials.gov Identifier: NCT01414179     History of Changes
Other Study ID Numbers: 2010-A00549-30
Study First Received: August 10, 2011
Last Updated: August 10, 2011
Health Authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)

Keywords provided by Central Hospital, Nancy, France:
nutrition
environnement
cardiovascular pathology

ClinicalTrials.gov processed this record on September 30, 2014