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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02905500
Other study ID # 2013/CHU/AVIRON
Secondary ID
Status Active, not recruiting
Phase N/A
First received September 12, 2016
Last updated September 14, 2016
Start date January 2014
Est. completion date January 2017

Study information

Verified date September 2016
Source Centre Hospitalier Universitaire de la Réunion
Contact n/a
Is FDA regulated No
Health authority France: Ethics Committee
Study type Observational

Clinical Trial Summary

AVIRON study aims at estimating the burden of various causes of death and morbidity in the Reunion Island population.


Description:

The identification of health priorities on a given territory is a major field of the research in Public health. The World Health Organization leads since the 1990s the "Global Burden of Disease" study. This study has for objective to estimate the burden of various causes of death and morbidity in a given population. It defines a standardized measure allowing the comparisons between the various countries. The measure developed internationally is the Disability-adjusted life year (DALY).

For the Indian Ocean zone, the international study provides values of DALYs for Madagascar, Seychelles and Mauritius. The estimation of DALYs for Reunion Island are based on data of mainland France and does not take into account specificities from Reunion Island. To better define Public health priorities, it seems essential to decline this measure at the regional level.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 800000
Est. completion date January 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- The whole population of Reunion Island

Exclusion Criteria:

- People not living in Reunion Island

Study Design

Observational Model: Ecologic or Community, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
France Centre Universitaire de La Réunion Saint Pierre

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de la Réunion

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of years of life lost or lived with disabilities 3 years No
Primary Prevalence of years of life lost or lived with disabilities 3 years No
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