St. Luke's-Roosevelt Hospital Center
New York, 10019, United States
NCT Number: NCT01837680
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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Notify Me18 year and older
Female
Interventional
Not applicable
New York, 10019, United States
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).
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: Insulin NPH, Insulin Levemir
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.
Time frame: up to 41 weeks
Number of each group that obtains glycemic control, defined as mean glucose <100mg/dl.
Time frame: up to 41 weeks
Time (weeks) to achieve glycemic control, as defined as mean glucose <100mg/dl
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
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.
Time frame: Number of pounds gained at each visit up to 41 weeks
Total weight gain in pregnancy
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
Time frame: at delivery, up to 41 weeks
Gestational age at delivery
Time frame: at delivery, up to 41 weeks
Number of participants with incidence of maternal hypoglycemia (<60mg/dl)
Time frame: at birth, up to 41 weeks
Percentage of neonatal hyperbilirubinemia - data not collected
Time frame: at birth, up to 41 weeks
Number of participants with incidence of neonatal intensive care unit admissions
Time frame: at birth, up to 41 weeks
method of delivery including cesarean section, vaginal delivery, or assisted vaginal delivery - data not collected
Time frame: at birth, up to 41 weeks
Number of live birth rate
Time frame: at birth, up to 41 weeks
Incidence of shoulder dystocia - data not collected
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
Time frame: at birth, up to 41 weeks
Number of participants with incidence of blood sugar <40mg/dl in neonate
St. Luke's-Roosevelt Hospital Center
Other
Insulin Detemir Versus Insulin NPH: A Randomized Prospective Study Comparing Glycemic Control in Pregnant Women With Diabetes
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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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