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Postpartum Screening of Type 2 Diabetes

Can we Screen Type 2 Diabetes on the 2nd Day After Delivery in Women Who Had Gestational Diabetes Mellitus?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01869608
Acronym
Tot ou tard
Enrollment
121
Registered
2013-06-05
Start date
2014-04-30
Completion date
2018-12-31
Last updated
2019-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes

Keywords

postpartum screening, type 2 diabetes

Brief summary

Gestational diabetes mellitus (GDM) complicates 5 to 30 % of pregnancies. GDM is defined as hyperglycemia with onset or first recognition during pregnancy. Because it is a forerunner of type 2 diabetes mellitus (T2DM), professional associations recommend T2DM postpartum screening (T2DM-pPS) at 6 weeks/6 months post delivery, using a 75g oral glucose tolerance test (OGTT). However, less than a quarter of these women are screened. This recommendation has failed for multiple reasons; the most important being that busy new mothers must deal with the major inconveniences of returning to a sampling center for a 2h testing session, bringing baby along or paying for a sitter, transportation, parking… A mother-friendly solution is direly needed. The investigators hypothesize that, in these women, results of an OGTT performed after delivery on the last day of their hospital stay (OGTT-1) will predict results of the recommended OGTT (OGTT-2) at 6 weeks/6 months postpartum. The main aim of our project is to determine the optimal cut-off value for the 2h glucose result during OGTT-1 in order to predict abnormal glucose tolerance status at OGTT-2 (the gold standard), in the same woman.

Interventions

PROCEDUREoral glucose tolerance test 2 days post-partum

Screening for type 2 diabetes after gestational diabetes mellitus.

Sponsors

The Lawson Foundation
CollaboratorOTHER
Université de Sherbrooke
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Women aged between 18 and 45 years; * Having a positive diagnosis of gestational diabetes mellitus (IADPSG criteria); * Treated with diet or insulin; * Have given birth to a child at term; gestational age \> 37 weeks; * Have been followed during her pregnancy by a physician who delivers in CHUS; * Have signed the consent form.

Exclusion criteria

* History of glucose intolerance or diabetes before the pregnancy; * Have presented another obstetrical pathology during the pregnancy; * Severe gestational high blood pressure with proteinuria; * Delayed intrauterine development syndrome; * Pregnancy with more than a foetus; * Drug addiction; * Had complications during the delivery such as: * Moderate to severe postpartum bleeding; * Surgery in postpartum (curettage, hysterectomy, etc.).

Design outcomes

Primary

MeasureTime frameDescription
Diagnosis of abnormal glucose tolerance12 weeks postpartumOral glucose tolerance test

Secondary

MeasureTime frameDescription
Patient's satisfaction12 weeks post-partumSatisfaction questionnaire

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026