About this trial
The objective of this study is to compare the accuracy of a 2hr glucose tolerance test administered during the postpartum hospitalization with the standard of care glucose tolerance testing (administered at 6 weeks postpartum). The primary hypothesis is that the glucose tolerance test administered in the postpartum period will be accurate and will improve compliance with postpartum testing for gestational diabetics.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Pregnant or recently postpartum (postpartum day 0 or 1)
≥ 18 years of age
Gestational age ≥34 weeks
A1 or A2 gestational diabetes
Disqualifiers
Medical exclusion from completing glucose tolerance testing
Steroid administration within 10 days prior to enrollment
Chronic steroid use
Trial population
All individual diagnosed with gestational diabetes will be approached following admission to labor and delivery and invited to participate.
Trial design
Cohort
Prospective
Treatments tested in this trial
Glucose tolerance test
Diagnostic testOral administration of a 75g glucose tolerance test during the postpartum hospitalization
Treatment groups
Trial outcomes
Primary outcomes
Accuracy of immediate glucose tolerance testing
Diagnostic accuracy between immediate postpartum glucose tolerance testing and gold standard testing
Secondary outcomes
Compliance with standard glucose tolerance testing
Percentage of the cohort that comply with glucose tolerance testing at their postpartum visit
Transition to primary care
Percentage of cohort that are appropriately referred to ongoing primary care
Sponsors and contacts
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