The catalog contains the description of the main databases in public health in France
July 30 2015
To assesses the impact of therapeutic education on reducing the risk and/or cardiovascular morbidity and mortality for hypertensive patients compared to regular follow-up.
Secondary objectives:
- To describe the development of cardiovascular risk score in the three groups over 5 years: individual education, collective education and control group (regular follow-up);
- To compare morbidity and mortality in the 3 groups;
- To compare the impact of individual or collective action against standard follow-up;
- To compare the results of individual action to collective action;
- To analyse the psychosocial profile of respondents to either method;
- To identify factors justifying the choice of either method or association;
- To describe and compare the quality of life of patients in the 3 groups.
July 30 2015
The project's general objective is to assess patient sensitivity to ischaemia/reperfusion (size of myocardial infarction, microvascular obstruction lesions, myocardial oedema) and post-conditioning response (ischaemic or pharmacological) in terms of:
- Clinical characteristics: comorbidities (diabetes, hypertension, smoking, heredity, pre-existing ischaemia);
- Biomarkers identified or to be identified (e.g. interleukin 17, angiopoietin-like 4, cyclophilin D).
January 27 2016
To estimate the frequency, severity and preventability of adverse events linked to ambulatory care, as well as investigate the context and contributing factors on the occurrence of these events and to estimate the hospital treatment costs.
July 30 2015
The objective of this registry is to provide a comprehensive catalogue of in vitro fertilisation activities in France (annual report on agency activity, regional analyses, etc..) and to assess the results, given associated factors such as:
- The woman (age they began smoking, indication of infertility, etc.);
- The man (smoking, indication of infertility, etc.);
- Attempt (number of attempts, gamete origin, technique used, quality of embryos, etc.);
The registry shall identify the donor couple's treatment path over several years, attempt by attempt, throughout different centres if required, and to provide recommendations in order to improve clinical practice for the patient;
To monitor pregnancy and to assess the child's health at birth through an after-birth study.
The catalog contains the description of the main databases in public health in France
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