Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT07233434

Screening for Type 2 Diabetes by Oral Glucose Tolerance Test in the Population Groups Not Diagnosed by Fasting Blood Glucose in Guadeloupe

Led by Centre Hospitalier Universitaire de la Guadeloupe · Updated on 2025-11-18

120

Participants Needed

1

Research Sites

391 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In France, only the fasting blood glucose (FBG) measurement is recommended for diabetes screening. Ethnic heterogeneity and genetic polymorphisms specific to the Afro-Caribbean and Indo-Caribbean population in Guadeloupe justify the interest to early screen type 2 diabetes mellitus (T2DM). Our main objective is to estimate the prevalence of T2DM defined by oral glucose tolerance (OGTT) in subjects with risk factors for T2DM and not diagnosed with the FBG.

CONDITIONS

Official Title

Screening for Type 2 Diabetes by Oral Glucose Tolerance Test in the Population Groups Not Diagnosed by Fasting Blood Glucose in Guadeloupe

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged over 18 and under 65 years
  • Subjects of African or Indian origin who self-identify as such
  • Normal fasting blood glucose levels below 110 mg/dL
  • HbA1c levels between 5.7% and 6.4%
  • Presence of one or more risk factors: BMI over 25 kg/m2, family history of type 2 diabetes in 1st or 2nd degree relatives, hypertension, or dyslipidemia
  • Affiliation to the national social health system or equivalent
  • Signed informed consent by the participant and investigator before any study exams
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding women
  • Women with a history of gestational diabetes
  • Diagnosis of polycystic ovary syndrome
  • Endocrine, liver, or kidney diseases affecting blood sugar control
  • Current treatment affecting glucose or insulin metabolism
  • Refusal to participate in the study
  • Inability to give informed consent due to impaired decision-making or legal guardianship
  • Participation in another ongoing research study with an exclusion period
  • Severe physical or psychological health issues that may affect study compliance

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Hospitalier Universitaire de la Guadeloupe

Pointe-à-Pitre, Guadeloupe, Guadeloupe, 97159

Actively Recruiting

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Research Team

V

Valérie HAMONY-SOTER

CONTACT

E

Eunice NUBRET

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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