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Real-time Continuous Glucose Monitoring

Primary Purpose

Gestational Diabetes

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Continuous glucose monitoring
Sponsored by
Eastern Virginia Medical School
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gestational Diabetes

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • maternal age 18 to 45
  • singleton gestation
  • gestational age less than 32 weeks gestation at study inclusion
  • BMI less than 45
  • 50g glucose challenge greater than 135 mg/dL
  • 100 g 3 hr oral glucose tolerance test greater than 2 abnormal values using the Carpenter Coustan cut offs (fasting greater than 95 mg/dL, 1 hr greater than 180 mg/dL, 2 hr greater than 155 mg/dL, 3 hr greater than 140 mg/dL)
  • attended the maternal-fetal medicine diabetes education class

Exclusion Criteria:

  • maternal age less than18 or greater than 45
  • multifetal gestation
  • gestational age greater than 32 weeks study inclusion
  • BMI greater than 45
  • pregestational diabetes
  • gestational diabetes diagnosed before 24 weeks
  • did not attend the diabetes education class
  • known fetal anomaly
  • known fetal aneuploidy
  • required ongoing treatment with medications that can exacerbate hyperglycemia (steroids, hydroxyprogesterone caproate injections (Makena), highly active antiretroviral therapy HIV medications)
  • learning disability
  • concern for non compliance with medical care
  • imminent preterm delivery due to maternal disease or fetal conditions
  • is not willing to wear CGM

Sites / Locations

  • Eastern Virginia Medical SchoolRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Blinded continuous glucose monitoring

Real time continuous glucose monitoring

Arm Description

The blinded CGM group will be using the Medtronic iPro2 system (Enlite sensor + iPro2 transmitter).

The real-time CGM group will be using the 530g system (inactivated 530g insulin pump (no insulin used, only used as display for CGM), Enlite sensor, MiniLink transmitter)

Outcomes

Primary Outcome Measures

Mean blood glucose (mg/dL)
Mean blood glucose (mg/dL) in the real-time CGM group compared to self-monitoring of blood glucose (SMBG) group during the 4th week of study from data collected on the 6 day of CGM use during that week.

Secondary Outcome Measures

Failed dietary therapy
Failed dietary therapy (started on medication),
Time spent in normoglycemia
Time spent in normoglycemia (min/day)
Time spent in hypoglycemia
Time spent in hypoglycemia (min/day)
BMI at time of delivery
BMI at time of delivery (kg/m2)
Gestational hypertension
Gestational hypertension (defined as systolic blood pressure > 140 mm Hg or diastolic blood pressure > 90 mmg Hg, on 2 occasions at least 4 hrs apart
Preeclampsia
Preeclampsia (defined as gestational hypertension plus either new-onset proteinuria (> 300 mg/24 2hrs, protein:creatinine > 0.3 mg/dL), thrombocytopenia (platelet count < 100,000/uL), elevated Aspartate aminotransferase or alanine aminotransferase (> 2x upper limit of normal), renal insufficiency (serum creatinine > 1.1 mg/dL or an unexplained doubling of creatinine), pulmonary edema, or cerebral or visual symptoms
HbA1C values
HbA1C values (%)
Polyhydramnios
Polyhydramnios (MVP > 8 cm at any point in the pregnancy)
Cesarean delivery
Cesarean delivery (w/ indication: macrosomia, malpresentation, failed induction, fetal distress, failed trial of labor after cesarean, scheduled repeat, other)
Induction of labor
Induction of labor (w/ indication)
Operative vaginal delivery
Operative vaginal delivery (yes/no) and type (forceps/vacuum)
Shoulder dystocia
Shoulder dystocia (diagnosed clinically)
Fetal macrosomia
Fetal macrosomia (> 4,000g at 38 wk u/s)
3rd or 4th degree perineal laceration
3rd or 4th degree perineal laceration at time of delivery
Gestational age at delivery
Gestational age at delivery (weeks, days)
Preterm delivery
Preterm delivery (< 37 weeks gestational age at birth)
Birth weight
Birth weight (grams)
Perinatal morbidity composite outcome
Hypoglycemia (yes/no): < 2 hrs after birth and before feeding, defined as < 35mg/dL Hyperbilirubinemia (yes/no): collected 16-36 hrs after birth, defined as > 95% for any given point after birth requiring phototherapy according to American Academy of Pediatrics guidelines Birth trauma (yes/no): brachial plexus injury or clavicular, humeral, or skull fracture Intrauterine fetal demise or neonatal death (yes/no): prior to hospital discharge
Large for gestational age
Large for gestational age (yes/no): defined as birth weight > 90%
Small for gestational age
Small for gestational age (yes/no): defined as birth weight < 10%
Admission to neonatal intensive care unit
Admission to neonatal intensive care unit (yes/no) and length of neonatal intensive care unit stay (days)
Respiratory distress syndrome
Respiratory distress syndrome (defined as need to supplemental oxygen > 4 hrs after birth)

Full Information

First Posted
October 25, 2017
Last Updated
November 21, 2017
Sponsor
Eastern Virginia Medical School
Collaborators
Medtronic
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1. Study Identification

Unique Protocol Identification Number
NCT03326232
Brief Title
Real-time Continuous Glucose Monitoring
Official Title
Real-time Continuous Glucose Monitoring for the Treatment of Gestational Diabetes: a Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 13, 2017 (Actual)
Primary Completion Date
July 2018 (Anticipated)
Study Completion Date
July 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Eastern Virginia Medical School
Collaborators
Medtronic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Gestational diabetes (GDM) is a condition of carbohydrate intolerance with onset or first recognition in pregnancy. The prevalence of GDM is as high as 25% in some populations and continues to rise with the increase in obesity and type-2 diabetes. GDM places the pregnancy at great risk to both the mother and the neonate. Recent studies have proven that interventions including dietary and medications lower the risk to the pregnancy. Both the American College of Obstetrics and Gynecology (ACOG) and the American Diabetes Association (ADA) recommend dietary interventions with daily glucose monitoring as the initial treatment of choice. Meanwhile, outside of pregnancy, promising new technologies such as continuous glucose monitors (CGM) are revolutionizing diabetic care. The investigators seek to determine if the constant feedback of a real-time CGM system would improve glycemic control compared to traditional management in GDM
Detailed Description
The investigators' proposed study will add new information to the emerging use of CGM in pregnant women with GDM. First, most studies only use CGM for 48 - 72hours at a time, while the investigators will be using CGM for 7 day intervals. Both groups will use the same Enlite sensor (Medtronic). The blinded CGM group will be using the Medtronic iPro2 system (Enlite sensor + transmitter). The real-time CGM group will be using the 530g system (iPro2 (Enlite sensor + transmitter) + inactivated 530g pump set only to display glucose values, no insulin will be administered). This CGM system has been FDA approved to for up to 7 days between sensor changes.26,27 Second, no previous study has used real time CGM in pregnant patients with GDM in the US. The investigators will be the first to describe the use of this technology in this patient population. Third, most of these trials have been performed on populations that are not representative of the investigators' patient population at EVMS. This will be the largest US study of CGM in GDM. Fourth wearable medical and fitness technology is already popular, but as both the technology and the demand continues to grow, it will become the future of diabetes management. Studies have already shown that real time CGM is an effective educational and motivational tool in type-1 and type-2 DM.28,29

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Blinded continuous glucose monitoring
Arm Type
Experimental
Arm Description
The blinded CGM group will be using the Medtronic iPro2 system (Enlite sensor + iPro2 transmitter).
Arm Title
Real time continuous glucose monitoring
Arm Type
Experimental
Arm Description
The real-time CGM group will be using the 530g system (inactivated 530g insulin pump (no insulin used, only used as display for CGM), Enlite sensor, MiniLink transmitter)
Intervention Type
Device
Intervention Name(s)
Continuous glucose monitoring
Intervention Description
The blinded CGM group will be using the Medtronic iPro2 system (Enlite sensor + iPro2 transmitter). The real-time CGM group will be using the 530g system (inactivated 530g insulin pump (no insulin used, only used as display for CGM), Enlite sensor, MiniLink transmitter)
Primary Outcome Measure Information:
Title
Mean blood glucose (mg/dL)
Description
Mean blood glucose (mg/dL) in the real-time CGM group compared to self-monitoring of blood glucose (SMBG) group during the 4th week of study from data collected on the 6 day of CGM use during that week.
Time Frame
week 1 vs. week 4
Secondary Outcome Measure Information:
Title
Failed dietary therapy
Description
Failed dietary therapy (started on medication),
Time Frame
week 1 vs. week 4
Title
Time spent in normoglycemia
Description
Time spent in normoglycemia (min/day)
Time Frame
week 1 vs. week 4
Title
Time spent in hypoglycemia
Description
Time spent in hypoglycemia (min/day)
Time Frame
week 1 vs. week 4
Title
BMI at time of delivery
Description
BMI at time of delivery (kg/m2)
Time Frame
BMI at time of delivery
Title
Gestational hypertension
Description
Gestational hypertension (defined as systolic blood pressure > 140 mm Hg or diastolic blood pressure > 90 mmg Hg, on 2 occasions at least 4 hrs apart
Time Frame
enrollement vs delivery.
Title
Preeclampsia
Description
Preeclampsia (defined as gestational hypertension plus either new-onset proteinuria (> 300 mg/24 2hrs, protein:creatinine > 0.3 mg/dL), thrombocytopenia (platelet count < 100,000/uL), elevated Aspartate aminotransferase or alanine aminotransferase (> 2x upper limit of normal), renal insufficiency (serum creatinine > 1.1 mg/dL or an unexplained doubling of creatinine), pulmonary edema, or cerebral or visual symptoms
Time Frame
enrollement vs delivery.
Title
HbA1C values
Description
HbA1C values (%)
Time Frame
HbA1C values week 1 compared to week 4 (%)
Title
Polyhydramnios
Description
Polyhydramnios (MVP > 8 cm at any point in the pregnancy)
Time Frame
Through study completion, an average of 9 months
Title
Cesarean delivery
Description
Cesarean delivery (w/ indication: macrosomia, malpresentation, failed induction, fetal distress, failed trial of labor after cesarean, scheduled repeat, other)
Time Frame
Delivery
Title
Induction of labor
Description
Induction of labor (w/ indication)
Time Frame
Delivery
Title
Operative vaginal delivery
Description
Operative vaginal delivery (yes/no) and type (forceps/vacuum)
Time Frame
Delivery
Title
Shoulder dystocia
Description
Shoulder dystocia (diagnosed clinically)
Time Frame
Delivery
Title
Fetal macrosomia
Description
Fetal macrosomia (> 4,000g at 38 wk u/s)
Time Frame
Most recent ultrasound before delivery
Title
3rd or 4th degree perineal laceration
Description
3rd or 4th degree perineal laceration at time of delivery
Time Frame
Delivery
Title
Gestational age at delivery
Description
Gestational age at delivery (weeks, days)
Time Frame
Delivery
Title
Preterm delivery
Description
Preterm delivery (< 37 weeks gestational age at birth)
Time Frame
Delivery
Title
Birth weight
Description
Birth weight (grams)
Time Frame
Delivery
Title
Perinatal morbidity composite outcome
Description
Hypoglycemia (yes/no): < 2 hrs after birth and before feeding, defined as < 35mg/dL Hyperbilirubinemia (yes/no): collected 16-36 hrs after birth, defined as > 95% for any given point after birth requiring phototherapy according to American Academy of Pediatrics guidelines Birth trauma (yes/no): brachial plexus injury or clavicular, humeral, or skull fracture Intrauterine fetal demise or neonatal death (yes/no): prior to hospital discharge
Time Frame
Delivery
Title
Large for gestational age
Description
Large for gestational age (yes/no): defined as birth weight > 90%
Time Frame
Delivery
Title
Small for gestational age
Description
Small for gestational age (yes/no): defined as birth weight < 10%
Time Frame
Delivery
Title
Admission to neonatal intensive care unit
Description
Admission to neonatal intensive care unit (yes/no) and length of neonatal intensive care unit stay (days)
Time Frame
Delivery
Title
Respiratory distress syndrome
Description
Respiratory distress syndrome (defined as need to supplemental oxygen > 4 hrs after birth)
Time Frame
Delivery

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Pregnant females with gestational diabetes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: maternal age 18 to 45 singleton gestation gestational age less than 32 weeks gestation at study inclusion BMI less than 45 50g glucose challenge greater than 135 mg/dL 100 g 3 hr oral glucose tolerance test greater than 2 abnormal values using the Carpenter Coustan cut offs (fasting greater than 95 mg/dL, 1 hr greater than 180 mg/dL, 2 hr greater than 155 mg/dL, 3 hr greater than 140 mg/dL) attended the maternal-fetal medicine diabetes education class Exclusion Criteria: maternal age less than18 or greater than 45 multifetal gestation gestational age greater than 32 weeks study inclusion BMI greater than 45 pregestational diabetes gestational diabetes diagnosed before 24 weeks did not attend the diabetes education class known fetal anomaly known fetal aneuploidy required ongoing treatment with medications that can exacerbate hyperglycemia (steroids, hydroxyprogesterone caproate injections (Makena), highly active antiretroviral therapy HIV medications) learning disability concern for non compliance with medical care imminent preterm delivery due to maternal disease or fetal conditions is not willing to wear CGM
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joanne Audouin, MS
Phone
757-446-5121
Email
audouij@evms.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Andrew Lane, MD
Phone
864-608-4134
Email
laneas@evms.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Malgorzata Mlynarczyk, MD, PhD
Organizational Affiliation
Eastern Virginia Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
Eastern Virginia Medical School
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23507
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joanne Audouin, MS
Phone
757-446-5121
Email
audouij@evms.edu
First Name & Middle Initial & Last Name & Degree
Andrew Lane, MD
Phone
864-608-4134
Email
laneas@evms.edu
First Name & Middle Initial & Last Name & Degree
Malgorzata Mlynarczyk, MD, PhD
First Name & Middle Initial & Last Name & Degree
Andrew Lane, MD
First Name & Middle Initial & Last Name & Degree
Margarita de Veciana, MD
First Name & Middle Initial & Last Name & Degree
Alfred Abuhamad, MD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Do not plan to share.
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Real-time Continuous Glucose Monitoring

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