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Evaluating for Type-2 Diabetes in the Very Early Postpartum Period

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Prediabetic State
Diabetes, Gestational
Diabetes Mellitus
Glucose Metabolism Disorders

Treatments

Other: Inpatient Postpartum GTT

Study type

Observational

Funder types

Other

Identifiers

NCT01988987
18-01705 (Other Identifier)
WUH 12318

Details and patient eligibility

About

Pregnancy-associated diabetes, known as gestational diabetes mellitus (GDM), is associated with an increased lifetime risk of developing diabetes mellitus (DM) or pre-diabetes. Up to 30% of women with GDM will continue have abnormal blood glucose tests 6 or more weeks after delivery. Early diagnosis and treatment of continued impaired glucose metabolism or DM is essential because serious health problems can result.

Current guidelines recommend a 75-gram, 2-hour glucose tolerance test (GTT) 6 or more weeks after delivery for women diagnosed with GDM in order to identify those with continued DM or impaired glucose metabolism. However, approximately half of these women do not get glucose testing after delivery. The ability to test women while they are still hospitalized after having a baby could greatly increase diagnosis, care and treatment of women with abnormal glucose metabolism.

Our objective is to determine if a 75-gram, 2-hour GTT administered to women with GDM two to four days after delivery can identify those who will have an abnormal GTT at 6-12 weeks after delivery.

Full description

This will be a prospective cohort study conducted at Winthrop-University Hospital. Women 18 years old or older who delivered a child or fetus within the previous 4 days at either hospital who also were diagnosed with GDM during the pregnancy will be eligible for participation. Women will be excluded if they have issues that would interfere with administration of a GTT, are unable /unwilling to provide informed consent, or cannot follow up. Anticipated enrollment will be 250 women at each study site.

While still hospitalized two to four days postpartum, subjects will undergo a 75-gram, 2-hour GTT and have blood tested for hemoglobin A1c and glucose levels. They will be reminded to do the recommended GTT 6-12 weeks after delivery. Maternal, neonatal, and obstetric characteristics will be collected, including the any GTT results. The results of the in-hospital GTT will be compared to the result of the GTT taken 6-12 weeks postpartum and tested for correlation.

Enrollment

123 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women 18 years old or older
  • Delivered a child or fetus within the previous 4 days
  • Diagnosed with gestational diabetes during the pregnancy

Exclusion criteria

  • Unable or unwilling to provide informed consent for the study
  • Unable to undergo or complete a 2-hour oral glucose tolerance test 2-4 days postpartum
  • Unable or unwilling to have study follow up.

Trial design

123 participants in 1 patient group

Inpatient Postpartum GTT
Description:
Women with gestational diabetes will undergo a 75 gram, 2 hour, oral glucose tolerance test 2-4 days postpartum prior to hospital discharge, in addition to undergoing the standard of care, outpatient glucose tolerance test performed 6-12 weeks postpartum
Treatment:
Other: Inpatient Postpartum GTT

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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