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Study of the Prevalence of Diabetes and Pre-diabetes in Réunion Island (PREVADIABRUN)

C

Centre Hospitalier Universitaire de la Réunion

Status

Enrolling

Conditions

Diabetes

Treatments

Diagnostic Test: Diabetes detection

Study type

Interventional

Funder types

Other

Identifiers

NCT06473584
2023/CHU/42

Details and patient eligibility

About

In view of the new priority given to diabetes in Réunion and the implementation of an ambitious plan to combat the disease at regional level, which includes the identification and management of pre-diabetes, the need for up-to-date data on the extent of these 2 diseases (diabetes and pre-diabetes) has become essential.

These two diseases have known risk factors: age, overweight, obesity, high waist circumference, family history, hypertension, eating habits and physical activity, all of which form part of a risk score for developing diabetes: the Findrisk recommended by the Haute Autorité de Santé for identifying people at risk of diabetes. Given the specific population characteristics of Réunion compared with Finland, where this score has been validated, it would seem important to be able to measure these risk indicators in the population as a function of carbohydrate status in order to check that the proposed thresholds are appropriate for the population of Réunion.

Finally, cardiovascular risk has been described as early as the pre-diabetes stage. Given the young age of onset of diabetes in Réunion and the high proportion of diagnoses of diabetes made following the occurrence of a cardiovascular complication, the study of the prognosis of carbohydrate status on the occurrence of complications using the social security information system will be offered on a voluntary basis to study subjects (via a probabilistic social security link).

Enrollment

2,000 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Have lived in Réunion island for at least one year
  • Be aged between 18 and 75
  • Affiliated to or benefiting from a social security scheme
  • Free, informed and signed consent

Exclusion criteria

  • No main residence on the island or fixed address for at least one year on the island
  • Participation in experimental research
  • Pregnant women
  • Adults under guardianship or legal protection
  • Not understanding French

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

2,000 participants in 1 patient group

Detection of glycaemic anomalies
Other group
Treatment:
Diagnostic Test: Diabetes detection

Trial contacts and locations

1

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Central trial contact

Catherine MARIMOUTOU, MD, PhD; Florence LEFEBVRE D'HELLENCOURT

Data sourced from clinicaltrials.gov

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