Early Intervention for Gestational Diabetes
Primary Purpose
Gestational Diabetes Mellitus
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Metformin
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Gestational Diabetes Mellitus focused on measuring GDM, Gestational Diabetes, Diabetes, Pregnancy
Eligibility Criteria
Inclusion Criteria:
Women delivered >37 weeks gestation in the Intermountain Healthcare Urban Central Region within the last 18 months to ascertain those at risk for GDM in their next pregnancy because of:
- A history of gestational diabetes in their immediately prior pregnancy
- A family history (i.e. type 2 diabetes in a first or second degree relative) of type 2 diabetes
- Delivery of an infant > 4000 gms.
- B.M.I. > 30 six months postpartum
- Hemoglobin A1C > 6.1% six months postpartum
Exclusion Criteria:
Pre-conception exclusion criteria will include any of the following:
- History of >1 miscarriage or fetal demise
- No contraindication to metformin (prior metformin intolerance, metabolic acidosis, GI disease)
- Hypertension (BP >135/85)
- No other endocrine, metabolic, renal, or autommune medical disorders
- Prior preterm birth
- Prior delivery complicated by shoulder dystocia
- Prior delivery complicated by neonatal palsy
- Multifetal pregnancy, including first-trimester embryonic demise of one or more
- Uterine malformations
- Illicit drug or alcohol abuse during current pregnancy
- Intent to deliver elsewhere
- Non-availability for prospective specimen/data collection
Sites / Locations
- Intermountain Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Metformin Placebo
Metformin
Arm Description
Outcomes
Primary Outcome Measures
Effect of metformin versus placebo on the development of GDM
Secondary Outcome Measures
Effects on maternal and fetal pregnancy outcomes of pre-conception metabolic intervention with metformin.
Full Information
NCT ID
NCT01171456
First Posted
July 13, 2010
Last Updated
January 15, 2013
Sponsor
Intermountain Health Care, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT01171456
Brief Title
Early Intervention for Gestational Diabetes
Official Title
Early Medical Intervention in Women at Risk for Gestational Diabetes
Study Type
Interventional
2. Study Status
Record Verification Date
January 2013
Overall Recruitment Status
Withdrawn
Why Stopped
Insufficient funding for enrollment of patients. The invesitgators realized the study could not be performed.
Study Start Date
April 2010 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Intermountain Health Care, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Gestational diabetes (GDM) represents a significant and growing source nationwide of morbidity and mortality for both mothers and infants. Between 5 and 10% of pregnancies are complicated by GDM. Infants exposed in utero to hyperglycemia from GDM have an increased risk of neonatal complications as well as an increased prevalence of a number of chronic diseases, including type 2 diabetes and schizophrenia. Recent research shows that treatment with metformin begun as soon as hyperglycemia is detected in pregnancy is safe and effective. Additional studies demonstrated that metformin is able to decrease the incidence of type 2 diabetes among individuals at risk for this disease. Based upon these findings, the investigators propose to test the hypothesis that metformin therapy for women at risk for gestational diabetes, started prior to conception and before the onset of hyperglycemia, both decreases the incidence of and improves the maternal and neonatal outcomes from GDM.
The investigators intend to conduct a prospective, randomized, double-blind placebo controlled range-finding study to measure the effects of early metabolic intervention with metformin in women at risk for GDM before the commencement of pregnancy or prior to completion of the first trimester. The target sample size for this pilot study is 100 women. The effect size observed will provide preliminary data for a subsequent study which will be sufficiently powered to detect small or moderate effects from early metabolic intervention in women at risk for GDM.
The specific aims of the proposed research consist of the following:
Determine whether treating women at risk for GDM with metformin prior to conception and/or completion of the 1st trimester decreases the incidence of GDM at 26 weeks' gestation.
Evaluate the effects on maternal and fetal pregnancy outcomes of pre-conception metabolic intervention with metformin in women at risk for GDM.
Use these pilot study results to:
identify specific demographic characteristics associated with an intervention effect
calculate effect size for specific outcomes
provide range-finding data for a subsequent study design
Metformin therapy for women at risk for gestational diabetes, started prior to conception and before the onset of hyperglycemia, both decreases the incidence of and improves the maternal and neonatal outcomes from GDM.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes Mellitus
Keywords
GDM, Gestational Diabetes, Diabetes, Pregnancy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Metformin Placebo
Arm Type
Placebo Comparator
Arm Title
Metformin
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Administration of Metformin or placebo prior to conception to prevent the onset of GDM.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Administration of Metformin or placebo prior to conception to prevent the onset of GDM.
Primary Outcome Measure Information:
Title
Effect of metformin versus placebo on the development of GDM
Time Frame
Pre-conception to delivery (at 8 week intervals)
Secondary Outcome Measure Information:
Title
Effects on maternal and fetal pregnancy outcomes of pre-conception metabolic intervention with metformin.
Time Frame
Pre-conception until discharge from hospital after delivery (at 4 week intervals)
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women delivered >37 weeks gestation in the Intermountain Healthcare Urban Central Region within the last 18 months to ascertain those at risk for GDM in their next pregnancy because of:
A history of gestational diabetes in their immediately prior pregnancy
A family history (i.e. type 2 diabetes in a first or second degree relative) of type 2 diabetes
Delivery of an infant > 4000 gms.
B.M.I. > 30 six months postpartum
Hemoglobin A1C > 6.1% six months postpartum
Exclusion Criteria:
Pre-conception exclusion criteria will include any of the following:
History of >1 miscarriage or fetal demise
No contraindication to metformin (prior metformin intolerance, metabolic acidosis, GI disease)
Hypertension (BP >135/85)
No other endocrine, metabolic, renal, or autommune medical disorders
Prior preterm birth
Prior delivery complicated by shoulder dystocia
Prior delivery complicated by neonatal palsy
Multifetal pregnancy, including first-trimester embryonic demise of one or more
Uterine malformations
Illicit drug or alcohol abuse during current pregnancy
Intent to deliver elsewhere
Non-availability for prospective specimen/data collection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ware Branch, M.D.
Organizational Affiliation
Intermountain Health Care, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Intermountain Medical Center
City
Murray
State/Province
Utah
ZIP/Postal Code
84107
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Early Intervention for Gestational Diabetes
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