Is it Possible to Screen for Type 2 Diabetes at Day 2 in Gestational Diabetes Mellitus Patients Postpartum?

NCT ID: NCT00921882

Last Updated: 2018-05-03

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

51 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-06-30

Study Completion Date

2013-05-31

Brief Summary

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Within 6 months of delivery, women who had gestational diabetes mellitus should be screened for type 2 diabetes with a fasting plasma glucose test and/or a 2-h postchallenge glycemia in a 75-g oral glucose tolerance test. However, not all women are screened. The objective of this study is to compare the screening test for type 2 diabetes done at 48 hours post-partum versus 8 weeks post-partum. The investigators want to measure the specificity, sensitivity, false and true predictive values of the screening test at 48 hours post-partum compared to the gold-standard.

Detailed Description

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Conditions

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Gestational Diabetes Mellitus Type 2 Diabetes

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Oral glucose tolerance test

oral glucose tolerance test performed 48 hours post-partum and 8 weeks post-partum.

Oral glucose tolerance test

Intervention Type PROCEDURE

Subjects will have the Oral glucose tolerance test 48 hours post-partum and the same test 8 weeks post-partum.

Interventions

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Oral glucose tolerance test

Subjects will have the Oral glucose tolerance test 48 hours post-partum and the same test 8 weeks post-partum.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Dx of gestational diabetes treated with insulin
* To be in post-partum
* Delivery of a baby of at least 37 weeks of gestation
* Have signed the consent form

Exclusion Criteria

* History of glucose intolerance of diabetes before the pregnancy
* Obstetrical pathology during pregnancy
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Université de Sherbrooke

OTHER

Sponsor Role lead

Responsible Party

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Jean-Luc Ardilouze

Endocrinologist, researcher

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jean-Luc Ardilouze, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Université de Sherbrooke

Locations

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Centre hospitalier universitaire de Sherbrooke

Sherbrooke, Quebec, Canada

Site Status

Countries

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Canada

Other Identifiers

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07-084

Identifier Type: -

Identifier Source: org_study_id

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