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Comparison of Two Screening Strategies for Gestational Diabetes (GDM2) (GDM2)

Primary Purpose

Gestational Diabetes, Pregnancy, Glucose Intolerance

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Gestational diabetes screening with fasting 3 hour 100 gm
Gestational diabetes screening with fasting 2 hour 75g
Sponsored by
Esa M Davis, MD MPH FAAFP
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Gestational Diabetes focused on measuring gestational diabetes screening, Carpenter Coustan Criteria, IADPSG criteria, Large for gestational age birth weight

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Pregnancy between 18-24 weeks of gestation
  • Singleton gestation
  • Planning to deliver at Magee-Womens Hospital, Pittsburgh, Pennsylvania

Exclusion Criteria:

  • Preexisting type 1 or 2 diabetes
  • Diabetes diagnosed at less than 24 weeks gestational age (GA)
  • Multiple gestations ( e.g. twins or triplets)
  • Hypertension requiring medications
  • Corticosteroid (IM, oral or IV) use in the 30 days prior to enrollment
  • Major congenital anomaly with anticipated preterm delivery due to maternal or fetal indications < 28 wks GA
  • Inability to complete the glucose testing before 30 completed weeks GA
  • Advanced HIV( on medications that cause hyperglycemia), severe liver disease, gastric bypass surgery or other illness/surgeries that preclude them from drinking the glucola solution.

Sites / Locations

  • UPMC- Magee Womens Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

3 hour 100 gm OGTT (CC Criteria)

2 hr 75 gm OGTT (IADPSG Criteria)

Arm Description

Gestational diabetes screening with fasting 3 hour 100 gm. Receive a fasting 3 hour 100 gram oral glucose tolerance test and are diagnosed based on the Carpenter Coustan Criteria: a 50 gm Glucose tolerance test of >130 + fasting 3 hour 100 gram oral glucose tolerance test with two or more values greater than the following diagnostic threshold: Fasting 95, 1-hour 180, 2-hour 155, or 3 hour 140 mg/dL . A positive criteria will be diagnostic for gestational diabetes.

Gestational diabetes screening with fasting 2 hour 75g. Receive a fasting 2 hour 75 gm oral glucose tolerance test and diagnosed based on the IADPSG which is if one or more values exceed the following diagnostic threshold: Fasting 92, 1-hour 180, or 2-hour 153 mg/dL.

Outcomes

Primary Outcome Measures

Large for Gestational Age (LGA) Infant
birth weight equal to or greater than the 90th percentile for gestational age and sex

Secondary Outcome Measures

Cesarean Delivery
the delivery of a baby through a surgical incision in the mother's abdomen and uterus
Maternal Composite Morbidity
maternal pre-eclampsia, 3rd or 4th degree vaginal lacerations, post-partum hemorrhage
Neonatal Composite Morbidity
1) hypoglycemia: blood glucose < 40mg/dl); 2) hyperbilirubinemia requiring treatment, clinical jaundice; 3)hyperinsulinemia- measured with c peptide level from venous cord blood; 4) still birth- absence of fetal heart tones before delivery, 5) birth trauma= Shoulder dystocia/brachial plexus injuries.

Full Information

First Posted
November 25, 2014
Last Updated
July 2, 2020
Sponsor
Esa M Davis, MD MPH FAAFP
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT02309138
Brief Title
Comparison of Two Screening Strategies for Gestational Diabetes (GDM2)
Acronym
GDM2
Official Title
Comparison of Two Screening Strategies for Gestational Diabetes (GDM2)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
August 11, 2015 (Actual)
Primary Completion Date
July 3, 2019 (Actual)
Study Completion Date
June 5, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Esa M Davis, MD MPH FAAFP
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a single site blinded RCT of 920 pregnant women with singleton gestation designed to compare the Carpenter-Coustan and IADPSG criteria for diagnosing gestational diabetes. Maternal metabolic profiles and infant growth will be assessed at randomization and at one year postpartum.
Detailed Description
Impaired glucose metabolism (gestational diabetes (GDM) and mild hyperglycemia) that occurs during pregnancy is associated with an increased risk for pregnancy complications and is also an early indication of long-term metabolic dysfunction leading to diabetes and cardiovascular disease. In the US, GDM is diagnosed using a two-step screening and diagnostic approach. The International Association of Diabetes and Pregnancy Study Group (IADPSG) proposed a one-step diagnostic approach that broadens the definition of GDM by lowering the cutoff values to include women with milder forms of hyperglycemia, who would have screened normal under the current two-step approach. The goal of these recommendations is better identification of women at risk for pregnancy complications and long-term metabolic dysfunction, but it results in a significant increase in the prevalence of GDM. The NIH GDM Consensus Development Conference committee does not recommend changing from the current two-step screening/diagnostic approach to the IADPSG one-step diagnostic approach without trials demonstrating that increasing the number of women diagnosed as having GDM results in better outcomes. We aim to 1) conduct a "real world" randomized controlled trial (RCT) to determine differences in short-term perinatal health outcomes between the two predominant GDM screening approaches, and 2) prospectively follow the mothers to examine their metabolic risk profiles and the growth of their infants at 1 year postpartum. Based on a pilot study, we propose a single site blinded RCT of 920 pregnant women ages 18-45 years without a diagnosis of diabetes, with a singleton pregnancy (18-24 wks gestation). Participants will have a non-fasting 1 hour 50 gm glucose challenge test (GCT) performed between 24-28 weeks' gestation. Women with 50 gm GCT results < 200 mg/dL will be randomized to receive either a fasting 2 hour 75 gm oral glucose tolerance test (OGTT) or a 3 hour 100 gm OGTT. GDM will be diagnosed using the IADPSG criteria for women receiving the 75 gm OGTT and Carpenter-Coustan criteria for women receiving the 100 gm. Participants and their physicians will be informed of the diagnosis of GDM, but blinded to the specific test results and diagnostic criteria. Participants with GDM will receive treatment from their primary provider. Questionnaires will be used to assess participants' and physicians' views on GDM testing. Metabolic profiles will be assessed at randomization and at a year postpartum. The primary outcome measure is large-for-gestational age fetal growth. The rationale for this RCT is that this is a unique opportunity to compare the two methods. At the end of the study, we will know whether women diagnosed at lower glucose levels with the IADPSG criteria are more likely to have adverse perinatal outcomes. We hypothesize that using IADPSG diagnostic criteria will result in greater detection of women with impaired glucose metabolism and treating these women will reduce adverse perinatal outcomes and prevent long-term metabolic dysfunction. This study will provide level A data for endorsing universal screening guidelines for GDM by major organizations and implementation into clinical care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes, Pregnancy, Glucose Intolerance
Keywords
gestational diabetes screening, Carpenter Coustan Criteria, IADPSG criteria, Large for gestational age birth weight

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
921 (Actual)

8. Arms, Groups, and Interventions

Arm Title
3 hour 100 gm OGTT (CC Criteria)
Arm Type
Active Comparator
Arm Description
Gestational diabetes screening with fasting 3 hour 100 gm. Receive a fasting 3 hour 100 gram oral glucose tolerance test and are diagnosed based on the Carpenter Coustan Criteria: a 50 gm Glucose tolerance test of >130 + fasting 3 hour 100 gram oral glucose tolerance test with two or more values greater than the following diagnostic threshold: Fasting 95, 1-hour 180, 2-hour 155, or 3 hour 140 mg/dL . A positive criteria will be diagnostic for gestational diabetes.
Arm Title
2 hr 75 gm OGTT (IADPSG Criteria)
Arm Type
Active Comparator
Arm Description
Gestational diabetes screening with fasting 2 hour 75g. Receive a fasting 2 hour 75 gm oral glucose tolerance test and diagnosed based on the IADPSG which is if one or more values exceed the following diagnostic threshold: Fasting 92, 1-hour 180, or 2-hour 153 mg/dL.
Intervention Type
Diagnostic Test
Intervention Name(s)
Gestational diabetes screening with fasting 3 hour 100 gm
Intervention Description
Participants receive fasting 3 hour 100 gm oral glucose tolerance test
Intervention Type
Diagnostic Test
Intervention Name(s)
Gestational diabetes screening with fasting 2 hour 75g
Intervention Description
Participants receive fasting 2 hour 75 gm oral glucose tolerance test
Primary Outcome Measure Information:
Title
Large for Gestational Age (LGA) Infant
Description
birth weight equal to or greater than the 90th percentile for gestational age and sex
Time Frame
at time of delivery
Secondary Outcome Measure Information:
Title
Cesarean Delivery
Description
the delivery of a baby through a surgical incision in the mother's abdomen and uterus
Time Frame
at delivery (approximately 40 weeks' gestation)
Title
Maternal Composite Morbidity
Description
maternal pre-eclampsia, 3rd or 4th degree vaginal lacerations, post-partum hemorrhage
Time Frame
at delivery (approximately 40 weeks' gestation)
Title
Neonatal Composite Morbidity
Description
1) hypoglycemia: blood glucose < 40mg/dl); 2) hyperbilirubinemia requiring treatment, clinical jaundice; 3)hyperinsulinemia- measured with c peptide level from venous cord blood; 4) still birth- absence of fetal heart tones before delivery, 5) birth trauma= Shoulder dystocia/brachial plexus injuries.
Time Frame
7 days after birth

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Pregnancy between 18-24 weeks of gestation Singleton gestation Planning to deliver at Magee-Womens Hospital, Pittsburgh, Pennsylvania Exclusion Criteria: Preexisting type 1 or 2 diabetes Diabetes diagnosed at less than 24 weeks gestational age (GA) Multiple gestations ( e.g. twins or triplets) Hypertension requiring medications Corticosteroid (IM, oral or IV) use in the 30 days prior to enrollment Major congenital anomaly with anticipated preterm delivery due to maternal or fetal indications < 28 wks GA Inability to complete the glucose testing before 30 completed weeks GA Advanced HIV( on medications that cause hyperglycemia), severe liver disease, gastric bypass surgery or other illness/surgeries that preclude them from drinking the glucola solution.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Esa M Davis, MD MPH
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
UPMC- Magee Womens Hospital
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Once the study is completed and the investigators have published the main manuscripts regarding the outcomes of the trial. De-identified data will be made available by request, review and approval of the investigators and the institution regulatory committee.
IPD Sharing Time Frame
Data will be shared in the appropriate time frame required by policy.
IPD Sharing Access Criteria
An application and review process will be implemented for accessing data.
Citations:
PubMed Identifier
28823926
Citation
Abebe KZ, Scifres C, Simhan HN, Day N, Catalano P, Bodnar LM, Costacou T, Matthew D, Illes A, Orris S, Duell J, Ly K, Davis EM. Comparison of Two Screening Strategies for Gestational Diabetes (GDM2) Trial: Design and rationale. Contemp Clin Trials. 2017 Nov;62:43-49. doi: 10.1016/j.cct.2017.08.012. Epub 2017 Aug 18.
Results Reference
background
PubMed Identifier
34259458
Citation
Davis EM, Abebe KZ, Simhan HN, Catalano P, Costacou T, Comer D, Orris S, Ly K, Decker A, Mendez D, Day N, Scifres CM. Perinatal Outcomes of Two Screening Strategies for Gestational Diabetes Mellitus: A Randomized Controlled Trial. Obstet Gynecol. 2021 Jul 1;138(1):6-15. doi: 10.1097/AOG.0000000000004431.
Results Reference
derived

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Comparison of Two Screening Strategies for Gestational Diabetes (GDM2)

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