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Intrapartum Glucose and Insulin Compared to Glucose Alone in Diabetic Women

Primary Purpose

Obstetric Labor, Pregnancy in Diabetics

Status
Recruiting
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
glucose solution and Insulin
glucose solution only
Sponsored by
HaEmek Medical Center, Israel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Obstetric Labor focused on measuring Gestational diabetes mellitus, Pre-gestational diabetes mellitus, Treatment, Neonatal hypoglycemia

Eligibility Criteria

18 Years - 60 Years (Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • HaEmek medical centerRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

glucose solution and insulin

glucose solution only

Arm Description

Participants will receive intravenous saline solution boosted with 5% glucose + 8 units regular insulin in a rate of 125 mL/h.

Participants will receive intravenous saline solution boosted with 5% glucose in a rate of 125 mL/h.

Outcomes

Primary Outcome Measures

Neonatal hypoglycemia
about 2-3 hours postpartum the neonate will have a capillary glucose test

Secondary Outcome Measures

Maternal glycemic control during labor
During labor glucose level will be obtained every hour. Average glucose level during labor will be calculated after labor.
Maternal urine ketones
Immediately post partum maternal urine will be checked for ketones
Total amount of regular insulin during labor
The total amount of regular insulin during labor will be calculated post partum
Mode of delivery
Mode of delivery
Length of delivery
Length of delivery
Breastfeeding
How many women breastfed in every study group
Neonatal APGAR score
Neonatal APGAR score
Umbilical cord PH
Umbilical cord PH
Umbilical cord glucose level
Umbilical cord glucose level
The need for neonatal IV glucose infusion
The need for neonatal IV glucose infusion
Neonatal jaundice
Neonatal jaundice- hyperbilirubinemia
Length of neonatal hospital stay
Length of neonatal hospital stay
NICU admission
NICU admission

Full Information

First Posted
September 4, 2017
Last Updated
October 8, 2023
Sponsor
HaEmek Medical Center, Israel
Collaborators
Holy Family Hospital, Nazareth, Israel
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1. Study Identification

Unique Protocol Identification Number
NCT03273881
Brief Title
Intrapartum Glucose and Insulin Compared to Glucose Alone in Diabetic Women
Official Title
Effect of Intrapartum Glucose With Compared to Without Constant Intravenous Insulin on Neonatal Hypoglycemia Among Diabetic Women. A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 31, 2017 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
HaEmek Medical Center, Israel
Collaborators
Holy Family Hospital, Nazareth, Israel

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstetric Labor, Pregnancy in Diabetics
Keywords
Gestational diabetes mellitus, Pre-gestational diabetes mellitus, Treatment, Neonatal hypoglycemia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
glucose solution and insulin
Arm Type
Active Comparator
Arm Description
Participants will receive intravenous saline solution boosted with 5% glucose + 8 units regular insulin in a rate of 125 mL/h.
Arm Title
glucose solution only
Arm Type
Active Comparator
Arm Description
Participants will receive intravenous saline solution boosted with 5% glucose in a rate of 125 mL/h.
Intervention Type
Drug
Intervention Name(s)
glucose solution and Insulin
Other Intervention Name(s)
Group 1
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
glucose solution only
Other Intervention Name(s)
Group 2
Intervention Description
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.
Primary Outcome Measure Information:
Title
Neonatal hypoglycemia
Description
about 2-3 hours postpartum the neonate will have a capillary glucose test
Time Frame
2-3 hours postpartum
Secondary Outcome Measure Information:
Title
Maternal glycemic control during labor
Description
During labor glucose level will be obtained every hour. Average glucose level during labor will be calculated after labor.
Time Frame
24 hours
Title
Maternal urine ketones
Description
Immediately post partum maternal urine will be checked for ketones
Time Frame
1 hour
Title
Total amount of regular insulin during labor
Description
The total amount of regular insulin during labor will be calculated post partum
Time Frame
24 hours
Title
Mode of delivery
Description
Mode of delivery
Time Frame
1 hour
Title
Length of delivery
Description
Length of delivery
Time Frame
24 hours
Title
Breastfeeding
Description
How many women breastfed in every study group
Time Frame
48 hours
Title
Neonatal APGAR score
Description
Neonatal APGAR score
Time Frame
5 minutes
Title
Umbilical cord PH
Description
Umbilical cord PH
Time Frame
30 minutes
Title
Umbilical cord glucose level
Description
Umbilical cord glucose level
Time Frame
30 minutes
Title
The need for neonatal IV glucose infusion
Description
The need for neonatal IV glucose infusion
Time Frame
48 hours
Title
Neonatal jaundice
Description
Neonatal jaundice- hyperbilirubinemia
Time Frame
48 hours
Title
Length of neonatal hospital stay
Description
Length of neonatal hospital stay
Time Frame
30 days
Title
NICU admission
Description
NICU admission
Time Frame
48 hours

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gali Gali, MD
Phone
972-4-6494035
Email
galit_ga@clalit.org.il
First Name & Middle Initial & Last Name or Official Title & Degree
Raed Salim, MD
Phone
972-4-6494355
Email
salim_ra@clalit.org.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gali Gali, MD
Organizational Affiliation
HaEmemk Medical Center, Afula, Israel.
Official's Role
Principal Investigator
Facility Information:
Facility Name
HaEmek medical center
City
Afula
ZIP/Postal Code
18101
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
galit Garmi, MD
Phone
97246494335
Email
galit_ga@clalit.org.il

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
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729447
Citation
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Results Reference
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Citation
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Citation
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Citation
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Intrapartum Glucose and Insulin Compared to Glucose Alone in Diabetic Women

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