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Completed

NCT Number: NCT01837680

Glycemic Control Using Insulin Levemir Versus Insulin NPH for Diabetes in Pregnancy

The aim of this study is to compare glycemic control in pregnant women treated with insulin Detemir and pregnant women treated with NPH insulin. These women are diagnosed with gestational diabetes (GDM) in the current pregnancy or have a preexisting diagnosis of type 2 diabetes (T2DM) at the onset of pregnancy. Our hypothesis is that there is no difference between these two treatment modalities in terms of glycemic control in diabetes.

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Key information

About this study

The experimental method will be a randomized controlled trial performed at Roosevelt Hospital in our Diabetes in Pregnancy Program (DIPP). Perinatologists managing the patient in DIPP determine when patients need further treatment with medical therapy. Patients undergoing care at DIPP may require medical intervention in the following clinical scenarios: failure of diet alone to control glycemic indices and grossly abnormal glucose tolerance screening test results suggesting disease of such severity that diet alone would not be sufficient. After verbally counseling the patient, she will be recruited for the study by the investigators. An extensive explanation of the objectives of the study will be presented to the patient, as well as written copies of the protocol and consent. After informed consent is given, patients will be randomized to management with either insulin NPH or detemir together with rapid acting insulin aspart (Novolog) with meals, as necessary. The primary outcome will be level of glycemic control defined as overall mean blood glucose in pregnancy. This is a well established measure of overall glycemic control that has been used in numerous publications in the obstetric literature on diabetes in pregnancy. Participants will be followed until they deliver, with an expected range of 6-16 weeks depending on when the patient was enrolled in the study. The mean glucose will be determined by the sum of average glucose at each visit divided by the number of visits).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • All pregnant women with a viable singleton or multiple gestation at ≤34 weeks with gestational diabetes diagnosed in their current pregnancy requiring medical therapy. "Early diagnosis" GDM patients will also be included; which is defined as a diagnosis made prior to 24 weeks.
  • Women with known preexisting type 2 diabetes that are in need of medical therapy.

Exclusion criteria

  • Patients <18 years of age
  • a diagnosis of GDM outside of the gestational age stated above
  • known allergy/prior adverse reaction to insulin NPH or insulin detemir.
  • type 1 diabetes

Treatment and study plan

Insulin

Drug

Other names: Insulin NPH, Insulin Levemir

Primary outcomes

  1. Glycemic Control

    Time frame: up to 41 weeks

    Overall mean glucose value of pregnancy. This will be determined by the sum of average glucose value at each visit, divided by the number of visits.

Secondary outcomes

  1. Number of Patients Obtaining Glycemic Control

    Time frame: up to 41 weeks

    Number of each group that obtains glycemic control, defined as mean glucose <100mg/dl.

  2. Time to Achieve Glycemic Control

    Time frame: up to 41 weeks

    Time (weeks) to achieve glycemic control, as defined as mean glucose <100mg/dl

  3. Average Fasting Glucose

    Time frame: up to 41 weeks

    Mean fasting blood glucose in pregnancy, as determined by the sum of the mean fasting glucose at each visit divided by the number of visits

  4. Post-prandial Blood Glucose

    Time frame: up to 41 weeks

    Mean post-prandial blood glucose in pregnancy, as defined as the sum of the average post-prandial blood glucose at each visit divided by the number of visits.

  5. Weight Gain

    Time frame: Number of pounds gained at each visit up to 41 weeks

    Total weight gain in pregnancy

  6. Neonatal Weight

    Time frame: At delivery, up to 41 weeks

    Neonatal weight was estimated for occurrence of neonatal macrosomia (≥4000g birth weight) and neonatal LGA(large for gestational age)(birth weight >90th percentile for gestational age

  7. Gestational Age at Delivery

    Time frame: at delivery, up to 41 weeks

    Gestational age at delivery

  8. Maternal Hypoglycemia

    Time frame: at delivery, up to 41 weeks

    Number of participants with incidence of maternal hypoglycemia (<60mg/dl)

  9. Neonatal Bilirubin

    Time frame: at birth, up to 41 weeks

    Percentage of neonatal hyperbilirubinemia - data not collected

  10. Intensive Care Admissions

    Time frame: at birth, up to 41 weeks

    Number of participants with incidence of neonatal intensive care unit admissions

  11. Delivery Mode

    Time frame: at birth, up to 41 weeks

    method of delivery including cesarean section, vaginal delivery, or assisted vaginal delivery - data not collected

  12. Birth Rate

    Time frame: at birth, up to 41 weeks

    Number of live birth rate

  13. Shoulder Dystocia

    Time frame: at birth, up to 41 weeks

    Incidence of shoulder dystocia - data not collected

  14. Polyhydramnios

    Time frame: at each visit in pregnancy up to 41 weeks

    Incidence of polyhydramnios (defined as amniotic fluid index (AFI)>20 or deepest vertical pocket ≥8) - data not collected

  15. Neonatal Hypoglycemia

    Time frame: at birth, up to 41 weeks

    Number of participants with incidence of blood sugar <40mg/dl in neonate

Sponsors and collaborators

Lead sponsor

St. Luke's-Roosevelt Hospital Center

Other

Registry information

Official study title

Insulin Detemir Versus Insulin NPH: A Randomized Prospective Study Comparing Glycemic Control in Pregnant Women With Diabetes

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Apr 23, 2013
Registry last updated
May 30, 2017

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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