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A Pragmatic Approach to Lower Diabetes Risk After Gestational Diabetes

Primary Purpose

Diabetes, Gestational, PreDiabetes, Diabetes Mellitus, Type 2

Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Metformin
Sponsored by
Tufts Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diabetes, Gestational focused on measuring gestational diabetes, diabetes risk, medical management, risk prevention, postpartum, diabetes, metformin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Women currently pregnant with planned delivery at Tufts Medical Center
  2. Gestational diabetes mellitus diagnosed during pregnancy
  3. ≥18 years of age
  4. Opted for the 2 hour 75 gram OGTT during postpartum hospitalization
  5. Willing and able to sign the informed consent

Exclusion Criteria:

  1. Unable to commit to required study visits for any reason.
  2. Contraindications to metformin

    • Liver disease
    • Impaired renal function (Creatinine Clearance> )
    • Congestive heart failure(CHF)
    • Taking drugs that could interfere with metformin metabolism
  3. Taking metformin outside of pregnancy
  4. Prescribed medications for chronic disease that affect glucose metabolism (e.g., long term oral steroids).
  5. Decided against the 2 hour 75 gram OGTT during postpartum hospitalization.
  6. Preexisting diabetes mellitus.

Sites / Locations

  • Tufts Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Metformin

Arm Description

Participants will be given a daily prescription of metformin for 12 months postpartum. At 12 months and again at 15 months (3 months off the drug), HbA1c and weight will be assessed.

Outcomes

Primary Outcome Measures

HbA1C
These results will be shared with participants and their providers. Any participants who accepted metformin but do not have diabetes will be asked to stop all study medication and no more study medication will be dispensed.
HbA1C
At 15 months postpartum, study participants with prediabetes will be seen again for their final study visit. The investigators intend to follow all participants for 3 months after metformin treatment ends for both safety reasons and efficacy reasons. If the metformin was masking diabetes, the investigators want the opportunity to identify those participants and refer them for treatment. Additionally, prior studies have not determined whether the benefits of metformin extend after the medication is discontinued (as indicated by the FDA when the investigators requested to use metformin in the first year postpartum).

Secondary Outcome Measures

Weight
Weight

Full Information

First Posted
March 3, 2022
Last Updated
March 27, 2023
Sponsor
Tufts Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05280496
Brief Title
A Pragmatic Approach to Lower Diabetes Risk After Gestational Diabetes
Official Title
Implementation of a Pragmatic Approach to Lower Diabetes Mellitus Risk After a Diagnosis of Gestational Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 1, 2022 (Actual)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tufts Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is testing whether daily metformin for 1 year postpartum can reduce risk of diabetes in patients who had gestational diabetes. Typical care for prediabetes after gestational diabetes is counseling on diet and lifestyle. This study is researching whether management of diabetes prevention is more effective with the drug metformin. This study will be conducted at Tufts Medical Center.
Detailed Description
Women with a history of gestational diabetes mellitus (GDM) represent a unique population who may benefit from metformin as much as lifestyle intervention; when metformin is prescribed to these women remote from delivery after a diagnosis of prediabetes, it reduces their risk of developing diabetes mellitus (DM) by up to 40% over 10 years. However, in the current system in which gestational diabetes diagnosis, prediabetes testing, and metformin prescription are temporally separated by months to years, less than 20% of postpartum women undergo prediabetes testing. When prediabetes is identified in women with a history of GDM, only 7.8% are prescribed metformin. Given the increasing public health burden of DM, there is an urgent need to remedy this problem and correct this deficiency in health care delivery that allows so many at-risk women to remain unidentified and untreated. Compelling preliminary data, confirmed at several other sites, indicates that the postpartum glucose tolerance test to identify individuals with prediabetes can be moved from 4-12 weeks postpartum to 1-4 days postpartum, when women are still hospitalized, with test compliance of 92% and no reduction in sensitivity or specificity for prediabetes. When individuals with a history of GDM and prediabetes are prescribed metformin, they experience a 50% reduction in DM risk and a 3 kg increase in weight loss over three years compared to placebo. If these same benefits are realized when metformin is initiated soon after delivery, then a simple change in postpartum care so that metformin is routinely prescribed at hospital discharge to women with a history of GDM and prediabetes could improve the health of thousands of women annually by decreasing the number of women who develop DM and fail to achieve postpartum weight loss. Each year in the United States, approximately 280,000 women are diagnosed with GDM. Without intervention, up to 70% of these women will develop diabetes mellitus (DM) over their lifetime, resulting in devastating health consequences and escalating health care costs. However, implementing a postpartum glucose tolerance test and intervening with metformin for those with prediabetes may be a cost-effective change to postpartum care that would result in a profound decrease in DM incidence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Gestational, PreDiabetes, Diabetes Mellitus, Type 2
Keywords
gestational diabetes, diabetes risk, medical management, risk prevention, postpartum, diabetes, metformin

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Metformin
Arm Type
Experimental
Arm Description
Participants will be given a daily prescription of metformin for 12 months postpartum. At 12 months and again at 15 months (3 months off the drug), HbA1c and weight will be assessed.
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin is used to lower blood sugar in patients with high blood sugar (diabetes).
Primary Outcome Measure Information:
Title
HbA1C
Description
These results will be shared with participants and their providers. Any participants who accepted metformin but do not have diabetes will be asked to stop all study medication and no more study medication will be dispensed.
Time Frame
12 months
Title
HbA1C
Description
At 15 months postpartum, study participants with prediabetes will be seen again for their final study visit. The investigators intend to follow all participants for 3 months after metformin treatment ends for both safety reasons and efficacy reasons. If the metformin was masking diabetes, the investigators want the opportunity to identify those participants and refer them for treatment. Additionally, prior studies have not determined whether the benefits of metformin extend after the medication is discontinued (as indicated by the FDA when the investigators requested to use metformin in the first year postpartum).
Time Frame
15 months
Secondary Outcome Measure Information:
Title
Weight
Time Frame
12 months
Title
Weight
Time Frame
15 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women currently pregnant with planned delivery at Tufts Medical Center Gestational diabetes mellitus diagnosed during pregnancy ≥18 years of age Opted for the 2 hour 75 gram OGTT during postpartum hospitalization Willing and able to sign the informed consent Exclusion Criteria: Unable to commit to required study visits for any reason. Contraindications to metformin Liver disease Impaired renal function (Creatinine Clearance> ) Congestive heart failure(CHF) Taking drugs that could interfere with metformin metabolism Taking metformin outside of pregnancy Prescribed medications for chronic disease that affect glucose metabolism (e.g., long term oral steroids). Decided against the 2 hour 75 gram OGTT during postpartum hospitalization. Preexisting diabetes mellitus.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alysa St. Charles, MA
Phone
617-636-9897
Email
astcharles1@tuftsmedicalcenter.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erika Werner, MD
Organizational Affiliation
Tufts Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tufts Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alysa St. Charles, MA
Phone
617-636-9897
Email
astcharles1@tuftsmedicalcenter.org
First Name & Middle Initial & Last Name & Degree
Erika Werner, MD, MS
First Name & Middle Initial & Last Name & Degree
Jennifer Ludgin, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25706240
Citation
Aroda VR, Christophi CA, Edelstein SL, Zhang P, Herman WH, Barrett-Connor E, Delahanty LM, Montez MG, Ackermann RT, Zhuo X, Knowler WC, Ratner RE; Diabetes Prevention Program Research Group. The effect of lifestyle intervention and metformin on preventing or delaying diabetes among women with and without gestational diabetes: the Diabetes Prevention Program outcomes study 10-year follow-up. J Clin Endocrinol Metab. 2015 Apr;100(4):1646-53. doi: 10.1210/jc.2014-3761. Epub 2015 Feb 23.
Results Reference
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PubMed Identifier
27735930
Citation
Carter EB, Tuuli MG, Odibo AO, Macones GA, Cahill AG. Prenatal visit utilization and outcomes in pregnant women with type II and gestational diabetes. J Perinatol. 2017 Feb;37(2):122-126. doi: 10.1038/jp.2016.175. Epub 2016 Oct 13.
Results Reference
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PubMed Identifier
28910846
Citation
Dinglas C, Muscat J, Heo H, Islam S, Vintzileos A. Immediate Postpartum Glucose Tolerance Testing in Women with Gestational Diabetes: A Pilot Study. Am J Perinatol. 2017 Oct;34(12):1264-1270. doi: 10.1055/s-0037-1606620. Epub 2017 Sep 14. No abstract available.
Results Reference
background
PubMed Identifier
20670225
Citation
Hedderson MM, Darbinian JA, Ferrara A. Disparities in the risk of gestational diabetes by race-ethnicity and country of birth. Paediatr Perinat Epidemiol. 2010 Sep;24(5):441-8. doi: 10.1111/j.1365-3016.2010.01140.x.
Results Reference
background
PubMed Identifier
25894024
Citation
Moin T, Li J, Duru OK, Ettner S, Turk N, Keckhafer A, Ho S, Mangione CM. Metformin prescription for insured adults with prediabetes from 2010 to 2012: a retrospective cohort study. Ann Intern Med. 2015 Apr 21;162(8):542-8. doi: 10.7326/M14-1773.
Results Reference
background
PubMed Identifier
18826999
Citation
Ratner RE, Christophi CA, Metzger BE, Dabelea D, Bennett PH, Pi-Sunyer X, Fowler S, Kahn SE; Diabetes Prevention Program Research Group. Prevention of diabetes in women with a history of gestational diabetes: effects of metformin and lifestyle interventions. J Clin Endocrinol Metab. 2008 Dec;93(12):4774-9. doi: 10.1210/jc.2008-0772. Epub 2008 Sep 30.
Results Reference
background
PubMed Identifier
32470456
Citation
Society for Maternal-Fetal Medicine (SMFM); Werner EF, Has P, Rouse D, Clark MA. Two-day postpartum compared with 4- to 12-week postpartum glucose tolerance testing for women with gestational diabetes. Am J Obstet Gynecol. 2020 Sep;223(3):439.e1-439.e7. doi: 10.1016/j.ajog.2020.05.036. Epub 2020 May 26.
Results Reference
background
PubMed Identifier
30060291
Citation
Werner EF, Has P, Kanno L, Sullivan A, Clark MA. Barriers to Postpartum Glucose Testing in Women with Gestational Diabetes Mellitus. Am J Perinatol. 2019 Jan;36(2):212-218. doi: 10.1055/s-0038-1667290. Epub 2018 Jul 30.
Results Reference
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PubMed Identifier
27120481
Citation
Werner EF, Has P, Tarabulsi G, Lee J, Satin A. Early Postpartum Glucose Testing in Women with Gestational Diabetes Mellitus. Am J Perinatol. 2016 Aug;33(10):966-71. doi: 10.1055/s-0036-1583193. Epub 2016 Apr 27. Erratum In: Am J Perinatol. 2016 Dec;33(14 ):1433-1434.
Results Reference
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PubMed Identifier
34495405
Citation
Whelan AR, Ayala NK, Werner EF. Postpartum Use of Weight Loss and Metformin for the Prevention of Type 2 Diabetes Mellitus: a Review of the Evidence. Curr Diab Rep. 2021 Sep 8;21(10):37. doi: 10.1007/s11892-021-01410-7.
Results Reference
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PubMed Identifier
23666593
Citation
Bennett WL, Liu SH, Yeh HC, Nicholson WK, Gunderson EP, Lewis CE, Clark JM. Changes in weight and health behaviors after pregnancies complicated by gestational diabetes mellitus: the CARDIA study. Obesity (Silver Spring). 2013 Jun;21(6):1269-75. doi: 10.1002/oby.20133. Epub 2013 May 13.
Results Reference
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Links:
URL
https://doi.org/10.2337/diacare.25.12.2165
Description
The Diabetes Prevention Program

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A Pragmatic Approach to Lower Diabetes Risk After Gestational Diabetes

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