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Intrapartum Glucose and Insulin Compared to Glucose Alone in Diabetic Women

Effect of Intrapartum Glucose With Compared to Without Constant Intravenous Insulin on Neonatal Hypoglycemia Among Diabetic Women. A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03273881
Enrollment
200
Registered
2017-09-06
Start date
2017-10-31
Completion date
2023-12-31
Last updated
2023-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstetric Labor, Pregnancy in Diabetics

Keywords

Gestational diabetes mellitus, Pre-gestational diabetes mellitus, Treatment, Neonatal hypoglycemia

Brief summary

This study aims to examine the effect of intrapartum treatment of diabetic women with combined glucose and constant insulin infusion compared to glucose alone on the incidence of neonatal hypoglycemia. Pregnant women with diabetes in pregnancy will be randomly divided during labor to 2 groups: group 1, will receive intravenous glucose with constant insulin infusion; group 2 will receive intravenous glucose alone. The primary outcome is the incidence of neonatal hypoglycemia.

Detailed description

About 2 to 9% of pregnant women are diagnosed with gestational diabetes. Peripartum complications attributed to diabetes include: birth trauma, neonatal hypoglycemia and hyperinsulinemia and neonatal hyperbilirubinemia. The incidence of neonatal hypoglycemia is about 40%. Strict glycemic control may lower the risk of neonatal complications. There is a lack of evidence on how to manage women with diabetes during labor. Previous studies recommended the use of intravenous saline solution boosted with 5% glucose and insulin as needed, glucose 5% with constant insulin infusion and others recommended the use lactated Ringer's solution. Most of these studies are either retrospective or have a small number of participants. In this study we will examine the effect of 2 different protocols on glycemic control during labor and the immediate neonatal period. Women in group 1, will receive intravenous saline solution boosted with 5% glucose and constant insulin infusion. Women in group 2, will receive intravenous saline solution boosted with 5% glucose alone. The desirable intrapartum glucose level will be 70 to 100 mg/dL. Glucose levels will be checked hourly. Women in both groups will receive additional insulin infusion in cases of glucose levels above 100 mg/dL. Additionally, the 5% glucose solution will be substitute with lactated Ringer's solution in cases of glucose levels above 140 mg/dL. Intravenous fluid regimens will be assigned according to a computer randomization sequence generation program. Women will randomly assigned to the 2 groups in a 1:1 ratio. The randomization sequence results will be kept in the delivery ward in a closed study box. Site investigators will enroll participants after confirming eligibility. The sequence will be concealed until intervention is assigned (and after obtaining a signed informed consent). Our hypothesis is that 5% glucose combined with constant insulin infusion will achieve better glycemic control and thus will lead to lower rate of neonatal hypoglycemia. In order to detect a reduction of neonatal hypoglycemia from 40% to 20%, 182 women will be needed in both groups in order to achieve a level of significance of 95% (α, 2-sided = 0.05) and a power of 80% (β = 0.2).

Interventions

DRUGglucose solution and Insulin

Women in group 1, will receive intravenous saline solution boosted with 5% glucose combined with 8 units of insulin at a rate of 125mL/h. The desirable intrapartum glucose level will be 70 to 100 mg/dL. Glucose levels will be checked hourly. Glucose level between 100-140 mg/dL will be treated with additional intravenous insulin, 1 units/hour. Glucose level between 141-160 mg/dL will be treated with intravenous insulin, 2 units/hour. Additionally, the 5% glucose solution will be substitute with lactated Ringer's solution. Glucose level between 161-200 mg/dL will be treated with intravenous insulin, 4 units/hour. Glucose level above 200 mg/dL will be treated with intravenous insulin, 6 units/hour.

DRUGglucose solution only

Women in group 2, will receive intravenous saline solution boosted with 5% glucose only, at a rate of 125mL/h. Women in this group will be treated similar to group 1 if glucose levels crossed over 100 mg/dL.

Sponsors

Holy Family Hospital, Nazareth, Israel
CollaboratorOTHER
HaEmek Medical Center, Israel
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* \>37 weeks gestation * gestational diabetes mellitus according to Carpenter and Coustan * pregestational diabetes mellitus

Exclusion criteria

* Intrauterine fetal death * estimated fetal weight\<10p * multiple gestation * major fetal malformations

Design outcomes

Primary

MeasureTime frameDescription
Neonatal hypoglycemia2-3 hours postpartumabout 2-3 hours postpartum the neonate will have a capillary glucose test

Secondary

MeasureTime frameDescription
Maternal urine ketones1 hourImmediately post partum maternal urine will be checked for ketones
Total amount of regular insulin during labor24 hoursThe total amount of regular insulin during labor will be calculated post partum
Mode of delivery1 hourMode of delivery
Length of delivery24 hoursLength of delivery
Breastfeeding48 hoursHow many women breastfed in every study group
Neonatal APGAR score5 minutesNeonatal APGAR score
Maternal glycemic control during labor24 hoursDuring labor glucose level will be obtained every hour. Average glucose level during labor will be calculated after labor.
Umbilical cord glucose level30 minutesUmbilical cord glucose level
The need for neonatal IV glucose infusion48 hoursThe need for neonatal IV glucose infusion
Neonatal jaundice48 hoursNeonatal jaundice- hyperbilirubinemia
Length of neonatal hospital stay30 daysLength of neonatal hospital stay
NICU admission48 hoursNICU admission
Umbilical cord PH30 minutesUmbilical cord PH

Countries

Israel

Contacts

Primary ContactGali Gali, MD
galit_ga@clalit.org.il972-4-6494035
Backup ContactRaed Salim, MD
salim_ra@clalit.org.il972-4-6494355

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026