Diagnostic Approaches in Gestational Diabetes and Impact of Ethnicity
NCT ID: NCT03117543
Last Updated: 2018-10-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
152 participants
OBSERVATIONAL
2016-03-31
Brief Summary
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The researchers will validate a new home-use OGTT system (hOGTT), which measures whole blood glucose in capillary blood ('finger-stick' sample), against the gold standard venous plasma glucose in pregnancy.
The researchers will also investigate the performance of glycated haemoglobin (HbA1c) in screening for GDM. HbA1c is used for diagnosis of diabetes outside of pregnancy, but is currently not recommended for screening for GDM.
The researchers will also investigate relationships between glucose measured in different samples (venous versus capillary), different fractions (plasma versus whole blood), and using different methods in pregnancy.
In a substudy the researchers will investigate: ethnic differences in HbA1c and other glycaemic markers; the contribution of fasting and postprandial glucose handling, diet and ethnicity on HbA1c; and ethnic differences in insulin responses to 75g OGTT in pregnancy.
The researchers will invite pregnant women between 16-34 weeks gestation to participate. The research involves one hospital visit for an OGTT. Participants will have venous blood samples taken fasting and at 1-hour and 2-hours, and at the same times finger-stick blood samples will be tested. The researchers will invite women of Black African, Black Caribbean and White European ethnicity to participate in a substudy in which participants will have extra blood taken and a diet assessment.
If the hOGTT provides accurate results in pregnancy, using it to perform OGTTs at home would make screening for GDM less expensive and more convenient and may facilitate universal screening for GDM. Understanding ethnic differences in HbA1c will help determine if HbA1c is a reliable screening tool for GDM in our ethnically diverse local population.
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
* Pregnant woman at least 18 years of age
* 16-34 weeks gestation.
* Booked for pregnancy care at a participating centre
* Able to give informed consent to participate
Substudy:
• Women who are of White European, Black African or Black Caribbean ethnicity.
Exclusion Criteria
* Unable to give informed consent
* Known pre-pregnancy diabetes
* GDM diagnosed in the current pregnancy
Substudy
In addition to main study criteria:
* Women known to have sickle cell anaemia or thalassaemia.
18 Years
FEMALE
No
Sponsors
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King's College London
OTHER
Collaboration for Leadership in Applied Health Research and Care, United Kingdom
UNKNOWN
King's College Hospital NHS Trust
OTHER
Responsible Party
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Principal Investigators
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Katharine F Hunt, MBBS MRCP
Role: PRINCIPAL_INVESTIGATOR
King's College Hospital NHS Trust
Locations
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Clinical Research Facility, King's College Hospital NHS Foundation Trust
London, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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15/LO/1494
Identifier Type: OTHER
Identifier Source: secondary_id
180588
Identifier Type: OTHER
Identifier Source: secondary_id
KCH16-035
Identifier Type: -
Identifier Source: org_study_id
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