Early Intervention for Gestational Diabetes

January 15, 2013 updated by: Ware Branch, Intermountain Health Care, Inc.

Early Medical Intervention in Women at Risk for Gestational Diabetes

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:

  1. 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.
  2. Evaluate the effects on maternal and fetal pregnancy outcomes of pre-conception metabolic intervention with metformin in women at risk for GDM.
  3. Use these pilot study results to:

    1. identify specific demographic characteristics associated with an intervention effect
    2. calculate effect size for specific outcomes
    3. 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.

Study Overview

Status

Withdrawn

Intervention / Treatment

Study Type

Interventional

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Utah
      • Murray, Utah, United States, 84107
        • Intermountain Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Metformin
Administration of Metformin or placebo prior to conception to prevent the onset of GDM.
Placebo Comparator: Metformin Placebo
Administration of Metformin or placebo prior to conception to prevent the onset of GDM.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Effect of metformin versus placebo on the development of GDM
Time Frame: Pre-conception to delivery (at 8 week intervals)
Pre-conception to delivery (at 8 week intervals)

Secondary Outcome Measures

Outcome Measure
Time Frame
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)
Pre-conception until discharge from hospital after delivery (at 4 week intervals)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ware Branch, M.D., Intermountain Health Care, Inc.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2010

Primary Completion (Actual)

July 1, 2010

Study Completion (Actual)

July 1, 2010

Study Registration Dates

First Submitted

July 13, 2010

First Submitted That Met QC Criteria

July 27, 2010

First Posted (Estimate)

July 28, 2010

Study Record Updates

Last Update Posted (Estimate)

January 16, 2013

Last Update Submitted That Met QC Criteria

January 15, 2013

Last Verified

January 1, 2013

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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