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Clinical Trial Summary

The aim of this study is to utilise ultrasound, using an established method for detecting NAFLD, to determine whether the presence of NAFLD in women with GDM, detected during routine scanning, is a marker of deterioration in glycaemic status post-partum. We propose to assess the relationship between NAFLD and surrogates for insulin resistance as well as glycaemic status, insulin sensitivity and β-cell function, after delivery. The study is not seeking to compare the incidence of T2DM between those with and without NAFLD. This would require a longer follow-up and larger cohort size. Instead, it aims to quantify the degree of early deterioration of glycaemic status in these groups using insulin resistance markers. This is a clinically important issue as a greater level of insulin resistance would in itself trigger clinical intervention, including vigilant follow-up and empowerment for proactive healthy life style changes, which have been shown to prevent diabetes development .


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04362540
Study type Observational
Source University Hospitals of North Midlands NHS Trust
Contact Keira Watts
Phone 01782
Email keira.watts@uhnm.nhs.uk
Status Recruiting
Phase
Start date May 5, 2019
Completion date December 30, 2024

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