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Completed

NCT Number: NCT00678080

Metformin Versus Insulin in Pregnant Women With Type 2 Diabetes

Pregnant women with type 2 diabetes mellitus (T2DM) are at increased risk for miscarriages, birth defects, large infants, and stillbirths. Maintaining blood sugars in the normal range decreases these pregnancy complications. We hypothesize that metformin will achieve similar levels of blood sugar control compared to insulin. In doing so, metformin will prevent the increased risk of pregnancy complications associated with T2DM in pregnancy. We propose a pilot study of a randomized, controlled trial of metformin versus insulin in the treatment of T2DM during pregnancy.

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Key information

Age range

18 year–52 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Valley Baptist Hospital, Brownsville, Texas, United States

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About this study

Pregnant women with type 2 diabetes mellitus (T2DM) are at increased risk for miscarriages, birth defects, large infants, and stillbirths. Maintaining blood sugars in the normal range decreases these pregnancy complications. Currently, insulin is the primary medication used to treat pregnant women with T2DM. However, it is administered by injection several times a day and compliance is low in health disparity populations with high rates of obesity and diabetes. Insulin also has the potential to lead to dangerously low blood sugars. Metformin is a medication than can be administered as pills and is not associated with dangerous low blood sugars. In addition, this insulin sensitizer is the medication of choice for women who are obese and have T2DM outside of pregnancy. We hypothesize that metformin will achieve similar levels of blood sugar control compared to insulin. In doing so, metformin will prevent the increased risk of pregnancy complications associated with T2DM in pregnancy. The aims of this study is to determine if in pregnant women with T2DM, metformin achieves similar glycemic control, and similar maternal and neonatal outcomes when compared to insulin. We propose a pilot study of a randomized, controlled trial of metformin versus insulin in the treatment of T2DM during pregnancy.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The onset of T2DM for less than 10 years prior to the onset of pregnancy by patient history
  • Treatment with diet or oral hypoglycemic agents prior to pregnancy.
  • Pregnancies less than 20 weeks of pregnancy. This gestational age was chosen to include those women who initiated prenatal care in the second trimester, but still have the ability to improve their hemoglobin A1C (primary outcome) with medical therapy prior to delivery.
  • Newly diagnosed diabetes in the first 20 weeks of pregnancy. These women likely have had diabetes prior to the onset of pregnancy. They do not qualify for the diagnosis of gestational diabetes which is typically made after 20 weeks of pregnancy. Diagnosis will be made based on an elevated fasting blood glucose greater than 105 mg/dL, a 50 gram glucola result greater than 200 mg/dL or an abnormal 3 hour glucola test prior to 20 weeks of pregnancy. An abnormal 3-hour glucola test is defined as 2 out of 4 abnormal values.
  • Hemoglobin A1C <9%

Exclusion criteria

  • Gestational age greater than 20 weeks
  • Multiple gestations (twins or more gestations)
  • Type 1 diabetes by patient history
  • Known fetal chromosomal or structural defects
  • Contraindications to the use of metformin including renal disease, liver disease, prior myocardial infarction or sepsis.
  • Those with a hemoglobin A1C greater than 9%.
  • On insulin at the start of pregnancy

Treatment and study plan

metformin

Drug

Metformin 500 mg orally daily increased as needed to maintain glycemic control until a maximum of 2500 daily

Other names: Glucophage

Insulin (NPH and Regular)

Drug

Insulin will be administered based on maternal gestational age and maternal weight using NPH and Regular insulin. It will be administered subcutaneously 3 times a day

Primary outcomes

  1. The Number of Participants Who Achieved a Hemoglobin A1C <7%

    Time frame: during third trimester

    The hemoglobin A1c level is an indicator of glycemic control-it indicates the average level of blood sugar over the past 2 to 3 months. Hemoglobin A1c levels 6.5% and higher indicate diabetes.

  2. The Number of Participants Who Achieved a Hemoglobin A1C <7%

    Time frame: at the time of delivery

    The hemoglobin A1c level is an indicator of glycemic control-it indicates the average level of blood sugar over the past 2 to 3 months. Hemoglobin A1c levels 6.5% and higher indicate diabetes.

Secondary outcomes

  1. Body Mass Index

    Time frame: at the time of delivery

  2. Number of Participants With Hypoglycemia

    Time frame: During pregnancy

    Defined as hypoglycemia as documented by neonatal chart based on health care provider description

  3. Number of Participants Who Failed Metformin Therapy

    Time frame: Duration of pregnancy

    Those whose glucose levels were above target range thereby needing insulin therapy

  4. Number of Participants Who Had a Cesarean Section

    Time frame: At the time of delivery

  5. Number of Participants With Fetus With Macrosomia

    Time frame: At the time of delivery

  6. Number of Participants With Shoulder Dystocia

    Time frame: At the time of delivery

  7. Number of Participants Who Had a Newborn With Respiratory Distress Syndrome

    Time frame: Neonatal period

  8. Number of Participants With Newborns Who Needed Neonatal Dextrose

    Time frame: Neonatal period

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Registry information

Official study title

A Randomized, Controlled Trial of Metformin Versus Insulin in Women With Type 2 Diabetes Mellitus During Pregnancy in a Population With Severe Health Disparities

Important dates

Study start
2008
Primary completion
2011
Study completion
2011
First posted
May 15, 2008
Registry last updated
Nov 28, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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