Genetic Causes of Gestational Diabetes in the Emirati Population

Status Recruiting

Clinical Trial Summary

The study aims to identify the number of MODY patients to be found among Emirati women with GDM as the incidence and prevalence of monogenic diabetes among this group of patients is unknown. This will enable improvements in diagnostics, treatment and the counselling of these women.

Clinical Trial Description

The present study aims to perform systematic genetic screening of genes known as the cause of MODY in women diagnosed with gestational diabetes to estimate the prevalence of MODY. This is important to understand the extent to which monogenic diabetes is encountered for the first time during pregnancy. Once women with MODY developing GDM have been identified, biomarkers to identify these women can be found which will assist the clinical process of performing genetic screening in the right subset of patients. Also for the women participating in the present study, this is of great importance as correct genetic diagnosis will provide them with the needed information to receive optimal treatment, correct plan for follow-up and a more accurate prognosis in relation to risk of future complication and therefore prevention of such. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03589092
Study type	Observational
Source	Imperial College London Diabetes Centre
Contact	Hinda Daggag, PhD
Phone	+971 2 404 0800
Email	hdaggag@icldc.ae
Status	Recruiting
Phase
Start date	January 1, 2017
Completion date	December 31, 2020

View Details

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