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CAPO: Continuous Glucose Monitoring in A2 Gestational Diabetes and Pregnancy Outcomes (CAPO)

Primary Purpose

Gestational Diabetes, Maternal Complication of Pregnancy

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Continuous Glucose Monitor
Routine Care
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Gestational Diabetes focused on measuring gestational diabetes, fetal or neonatal outcomes, maternal morbidity

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • women between 18-50 years old
  • pregnant
  • singleton gestation
  • diagnosis of gestational diabetes requiring medication (A2) during the current pregnancy between 24-36 weeks' gestation

Exclusion Criteria:

  • pregestational diabetes
  • diagnosis with gestational diabetes < 24 weeks gestation or > 36 weeks gestation
  • known fetal anomalies
  • fetal growth restriction diagnosed during the current pregnancy
  • diagnosis of polyhydramnios at time of randomization
  • abnormal diagnostic genetic testing or genetic screening for the fetus in the current pregnancy prior to randomization
  • twin or higher order multiple gestation
  • non-compliance with prenatal visits (missing ≥3 visits prior to enrollment) prior to diagnosis with A2 gestational diabetes
  • maternal medical comorbidities including the following: lupus, chronic hypertension, cancer, ischemic cardiovascular disease

Sites / Locations

  • Yale UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Routine Care

Continuous Glucose Monitor

Arm Description

Monitoring of control of gestational diabetes with routine care and use of a glucometer and fingersticks 4 times a day

Monitoring of control of gestational diabetes with use of a continuous glucose monitor

Outcomes

Primary Outcome Measures

Composite Primary Outcome
The number of participants who have at least one of each of the following outcome measures occur: perinatal death, shoulder dystocia, birth weight greater than 4,000 grams, NICU admission for treatment of hypoglycemia (blood glucose level <40mg/dL) and birth trauma, including fracture or nerve palsy. Any one of these would make the composite primary outcome positive and will be recorded as a categorical variable.

Secondary Outcome Measures

cesarean delivery for an arrest of labor disorder
The number of women who undergo a cesarean delivery for arrest of dilation or descent during labor or induction of labor. This will be recorded as a categorical (yes/no) variable
hypertensive disorders of pregnancy.
The number of women who receive a diagnosis of a hypertensive disorder of pregnancy (gestational hypertension, preeclampsia, HELLP). This will be recorded as a categorical (yes/no) variable

Full Information

First Posted
January 2, 2020
Last Updated
February 6, 2023
Sponsor
Yale University
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1. Study Identification

Unique Protocol Identification Number
NCT04219085
Brief Title
CAPO: Continuous Glucose Monitoring in A2 Gestational Diabetes and Pregnancy Outcomes
Acronym
CAPO
Official Title
CAPO: Continuous Glucose Monitoring in A2 Gestational Diabetes and Pregnancy Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2020 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will utilize continuous glucose monitoring in women with A2 gestational diabetes. Women will be randomized to continuous glucose monitoring or routine care with fingersticks to check their blood glucose four times daily. It is hypothesized that women in the continuous glucose monitoring arm will have a lower incidence of the composite primary outcome, which includes the following variables: perinatal death, shoulder dystocia, birth weight greater than 4,000 grams, NICU admission for treatment of hypoglycemia (blood glucose level <40mg/dL) and birth trauma, including fracture or nerve palsy.
Detailed Description
Diabetes complicates 6-7% of pregnancies annually and approximately 85% of these cases are women diagnosed with gestational diabetes (GDM).1,2 The prevalence of GDM varies within populations based on obesity rates, maternal age and ethnicity. GDM is diagnosed during the third trimester through a two-step process of a 50-gram oral glucose challenge screen and a subsequent 100-gram oral glucose challenge test if the woman screens positive. Once the diagnosis is confirmed women are asked to monitor their glucose levels with finger sticks at least four times a day (fasting and post-prandial) and medication is added when glucose target goals cannot be reached by diet and exercise alone. Approximately, 15% of women will not reach glucose target goals with diet and exercise alone and will require medication. These women are then diagnosed with class A2 GDM by the White classification of diabetes. Identification of women with GDM who require treatment is essential in optimizing pregnancy outcomes for these women. Treatment of GDM results in lower neonatal morbidity, reduced incidence of large for gestational age infants (LGA), reduced incidence of preeclampsia and shoulder dystocia and a reduced need for cesarean delivery.3-5 Since LGA infants are at higher risk for hypoglycemia which may necessitate admission to the neonatal intensive care unit (NICU), treatment of GDM reduces the incidence of LGA infants resulting in less hypoglycemia and NICU admissions. Given that pregnancy outcomes are directly tied to blood glucose control, it is essential that women with GDM play an active role in the monitoring of their disease. The frequency of monitoring and frustration with diet can lead to issues with patient compliance and ultimately impact their pregnancy outcomes. One study found that just over half of women successfully tested their blood glucose via finger sticks ≥ 80% of the time. About 25% of the women in the same study had <90% of the values matching in their glucometer and their blood glucose log.6 Given these issues with compliance the need for a better and more convenient monitoring system is evident. Continuous glucose monitors (CGM) are a relatively new device that have yet to be fully explored for their utility in pregnancy. The current generation of CGM has had exponential growth in the clinical care of diabetes, driven primarily by the improved accuracy of these devices, longer duration sensor life (ranging from 7-14 days in currently available models), and the ability to collect these data without performing calibration of the sensors with fingerstick glucose readings. Continuous Glucose Monitoring in Women with Type 1 Diabetes in Pregnancy Trial (CONCEPTT), demonstrated the utility of CGM data to decrease the frequency of adverse neonatal outcomes in a pregestational diabetes population.7 A more recent trial of blinded CGM data in women with GDM showed mean sensor glucose was significantly higher in women who delivered LGA infants. The 24-hour mean glucose was different between groups in this study (112 mg/dL vs. 104 mg/dL, p=0.025), driven by higher overnight mean glucose levels (108 mg/dL vs. 99 mg/dL, p=0.005).8 Given that this is not a time that women with GDM would normally be monitoring their blood sugar it is evident that CGM may be useful, not only in increasing patient compliance by eliminating the need for measuring serum glucose via finger sticks and a glucometer four times a day but by allowing for monitoring of blood glucose levels at times that are not normally convenient for testing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes, Maternal Complication of Pregnancy
Keywords
gestational diabetes, fetal or neonatal outcomes, maternal morbidity

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
randomized controlled trial, not blinded
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Routine Care
Arm Type
Active Comparator
Arm Description
Monitoring of control of gestational diabetes with routine care and use of a glucometer and fingersticks 4 times a day
Arm Title
Continuous Glucose Monitor
Arm Type
Experimental
Arm Description
Monitoring of control of gestational diabetes with use of a continuous glucose monitor
Intervention Type
Device
Intervention Name(s)
Continuous Glucose Monitor
Intervention Description
Wearing of a continuous glucose monitor to monitor blood glucose levels in women with gestational diabetes
Intervention Type
Other
Intervention Name(s)
Routine Care
Intervention Description
Use of a glucometer to monitor blood glucose levels in women with gestational diabetes
Primary Outcome Measure Information:
Title
Composite Primary Outcome
Description
The number of participants who have at least one of each of the following outcome measures occur: perinatal death, shoulder dystocia, birth weight greater than 4,000 grams, NICU admission for treatment of hypoglycemia (blood glucose level <40mg/dL) and birth trauma, including fracture or nerve palsy. Any one of these would make the composite primary outcome positive and will be recorded as a categorical variable.
Time Frame
from enrollment up until delivery by 40 weeks gestation
Secondary Outcome Measure Information:
Title
cesarean delivery for an arrest of labor disorder
Description
The number of women who undergo a cesarean delivery for arrest of dilation or descent during labor or induction of labor. This will be recorded as a categorical (yes/no) variable
Time Frame
during delivery by 40 weeks gestation
Title
hypertensive disorders of pregnancy.
Description
The number of women who receive a diagnosis of a hypertensive disorder of pregnancy (gestational hypertension, preeclampsia, HELLP). This will be recorded as a categorical (yes/no) variable
Time Frame
from enrollment, through delivery by 40 weeks gestation and the immediate postpartum hospitalization up to 7 days postpartum

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
ongoing pregnancy is required for study
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: women between 18-50 years old pregnant singleton gestation diagnosis of gestational diabetes requiring medication (A2) during the current pregnancy between 24-36 weeks' gestation Exclusion Criteria: pregestational diabetes diagnosis with gestational diabetes < 24 weeks gestation or > 36 weeks gestation known fetal anomalies fetal growth restriction diagnosed during the current pregnancy diagnosis of polyhydramnios at time of randomization abnormal diagnostic genetic testing or genetic screening for the fetus in the current pregnancy prior to randomization twin or higher order multiple gestation non-compliance with prenatal visits (missing ≥3 visits prior to enrollment) prior to diagnosis with A2 gestational diabetes maternal medical comorbidities including the following: lupus, chronic hypertension, cancer, ischemic cardiovascular disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Audrey Merriam, MD, MS
Phone
(203) 688-2800
Email
audrey.merriam@yale.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Audrey Merriam, MD, MS
Organizational Affiliation
Assistant Professor; Assistant Professor, Department of Obstetrics, Gynecology and Reproductive Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yale University
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06511
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Audrey Merriam, MD, MS
Phone
203-688-2800
Email
audrey.merriam@yale.edu

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
no plan to share
Citations:
PubMed Identifier
30707672
Citation
Martin JA, Hamilton BE, Osterman MJK, Driscoll AK, Drake P. Births: Final Data for 2017. Natl Vital Stat Rep. 2018 Nov;67(8):1-50.
Results Reference
background
Citation
The American College of Obstetricians and Gynecologists Practice Bulletin Number 190. Gestational Diabetes Mellitus. February 2018.
Results Reference
background
PubMed Identifier
15951574
Citation
Crowther CA, Hiller JE, Moss JR, McPhee AJ, Jeffries WS, Robinson JS; Australian Carbohydrate Intolerance Study in Pregnant Women (ACHOIS) Trial Group. Effect of treatment of gestational diabetes mellitus on pregnancy outcomes. N Engl J Med. 2005 Jun 16;352(24):2477-86. doi: 10.1056/NEJMoa042973. Epub 2005 Jun 12.
Results Reference
background
PubMed Identifier
19797280
Citation
Landon MB, Spong CY, Thom E, Carpenter MW, Ramin SM, Casey B, Wapner RJ, Varner MW, Rouse DJ, Thorp JM Jr, Sciscione A, Catalano P, Harper M, Saade G, Lain KY, Sorokin Y, Peaceman AM, Tolosa JE, Anderson GB; Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network. A multicenter, randomized trial of treatment for mild gestational diabetes. N Engl J Med. 2009 Oct 1;361(14):1339-48. doi: 10.1056/NEJMoa0902430.
Results Reference
background
PubMed Identifier
23712381
Citation
Hartling L, Dryden DM, Guthrie A, Muise M, Vandermeer B, Donovan L. Benefits and harms of treating gestational diabetes mellitus: a systematic review and meta-analysis for the U.S. Preventive Services Task Force and the National Institutes of Health Office of Medical Applications of Research. Ann Intern Med. 2013 Jul 16;159(2):123-9. doi: 10.7326/0003-4819-159-2-201307160-00661.
Results Reference
background
PubMed Identifier
28724718
Citation
Cosson E, Baz B, Gary F, Pharisien I, Nguyen MT, Sandre-Banon D, Jaber Y, Cussac-Pillegand C, Banu I, Carbillon L, Valensi P. Poor Reliability and Poor Adherence to Self-Monitoring of Blood Glucose Are Common in Women With Gestational Diabetes Mellitus and May Be Associated With Poor Pregnancy Outcomes. Diabetes Care. 2017 Sep;40(9):1181-1186. doi: 10.2337/dc17-0369. Epub 2017 Jul 19.
Results Reference
background
PubMed Identifier
31221709
Citation
Law GR, Alnaji A, Alrefaii L, Endersby D, Cartland SJ, Gilbey SG, Jennings PE, Murphy HR, Scott EM. Response to Comment on Law et al. Suboptimal Nocturnal Glucose Control Is Associated With Large for Gestational Age in Treated Gestational Diabetes Mellitus. Diabetes Care 2019;42:810-815. Diabetes Care. 2019 Jul;42(7):e123-e124. doi: 10.2337/dci19-0018. No abstract available.
Results Reference
background
PubMed Identifier
28923465
Citation
Feig DS, Donovan LE, Corcoy R, Murphy KE, Amiel SA, Hunt KF, Asztalos E, Barrett JFR, Sanchez JJ, de Leiva A, Hod M, Jovanovic L, Keely E, McManus R, Hutton EK, Meek CL, Stewart ZA, Wysocki T, O'Brien R, Ruedy K, Kollman C, Tomlinson G, Murphy HR; CONCEPTT Collaborative Group. Continuous glucose monitoring in pregnant women with type 1 diabetes (CONCEPTT): a multicentre international randomised controlled trial. Lancet. 2017 Nov 25;390(10110):2347-2359. doi: 10.1016/S0140-6736(17)32400-5. Epub 2017 Sep 15. Erratum In: Lancet. 2017 Nov 25;390(10110):2346.
Results Reference
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CAPO: Continuous Glucose Monitoring in A2 Gestational Diabetes and Pregnancy Outcomes

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