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Early Detection of Gestational Diabetes Mellitus in Pregnancy

Primary Purpose

Gestational Diabetes Mellitus in Pregnancy, Pregnancy, High Risk

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Enhanced First Trimester GDM Screening
Routine Gestational Diabetes Screening
Sponsored by
University of Massachusetts, Worcester
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Gestational Diabetes Mellitus in Pregnancy focused on measuring Pregnancy, Gestational Diabetes, Screening, Maternal Outcomes, Neonatal Outcomes

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • 1) age greater than or equal to 18 years old,
  • 2) singleton gestation less than or equal to 12 weeks at initial obstetric visit,
  • 3) receiving prenatal care at UMMHC and plans to deliver at UMMHC,
  • 4) able and willing to provide informed consent,
  • 5) English or Spanish speaking, and
  • 6) are at high risk for developing GDM by ACOG clinical risk factor guidelines.

Exclusion Criteria:

  • 1) known diagnosis of pre-existing pregestational diabetes,
  • 2) plan to receive prenatal care or deliver outside of UMMHC,
  • 3) inability to complete oral glucose tolerance test (e.g. gastric bypass surgery history, gastric dumping syndrome history, vomiting of oral glucose tolerance test), or
  • 4) systemic steroid use.

Sites / Locations

  • University of Massachusetts Memorial Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Enhanced First Trimester GDM Screening

Standard of Care GDM Screening

Arm Description

Women who are randomly assigned to this condition will be required to have early glucose screening with a prediction model composed of additional clinical risk factors and serum biomarkers (triglycerides, PAPP-A, and lipocalin-2) with their initial prenatal laboratory assessment.

Women who will be randomized to the comparison condition of usual standard of care will undergo routine standard of care. The standard of care will consist of routine screening for diabetes in pregnancy between 24 to 28 weeks of gestation via the two-step screening method with possible early screening with either plasma fasting glucose, oral glucose tolerance test, or hemoglobin A1c at the providers discretion to represent true clinical practice.

Outcomes

Primary Outcome Measures

Gestational Diabetes Mellitus
Confirmed diagnosis of GDM based on 3 hour 100 gram glucose tolerance test

Secondary Outcome Measures

Mode of Delivery
Mode of delivery (Vaginal versus Cesarean delivery)
Neonatal Birthweight
Neonatal Birthweight
Number of Participants with Shoulder Dystocia
Number of Participants with Shoulder Dystocia
Number of participants with brachial plexus injury
Number of participants with brachial plexus injury
APGAR Score
APGAR Score (range 0 to 10, with 10 being the best)
Neonatal Intensive Care Unit Admission
Admission to Level 2 or greater neonatal ICU and length of stay
Gestational Age at Delivery
Gestational Age at Delivery
Patient Satisfaction with Diabetes Screening Method
This will be assessed by the Patient Satisfaction Survey questionnaire, which is scored out of 30, with 30 being the highest score)

Full Information

First Posted
May 18, 2022
Last Updated
October 8, 2023
Sponsor
University of Massachusetts, Worcester
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1. Study Identification

Unique Protocol Identification Number
NCT05388643
Brief Title
Early Detection of Gestational Diabetes Mellitus in Pregnancy
Official Title
Early Detection of Gestational Diabetes Mellitus in Pregnancy: A Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2024 (Anticipated)
Primary Completion Date
July 1, 2025 (Anticipated)
Study Completion Date
December 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Massachusetts, Worcester

4. Oversight

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

5. Study Description

Brief Summary
The purpose of this study is to develop an implementation protocol and test the feasibility and acceptability of a first trimester screening protocol for the early detection of gestational diabetes mellitus (GDM).
Detailed Description
Gestational diabetes mellitus (GDM) is an important contributor to both maternal and neonatal morbidity and mortality in pregnancy. GDM has lifelong complications including an increased risk of developing type 2 diabetes mellitus and cardiovascular disease for women, and their offspring are at higher risk of being obese and also having diabetes in childhood and adolescence. Approximately 1 in 8 pregnancies is impacted by gestational diabetes mellitus worldwide. First trimester GDM screening is varied due to conflicting national guidelines, and the best strategy is unknown. The goal of the proposed research is to develop an implementation protocol and test the feasibility and acceptability of a first trimester screening protocol for the early detection of GDM. The investigators will utilize a pilot randomized controlled trial to recruit 80 high-risk pregnant women in the first trimester, of whom half will receive protocolized early GDM screening with serum biomarkers before 12 weeks and the remaining half will receive the current standard of care with screening between 24 and 28 weeks of gestation with possible early screening based on provider discretion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes Mellitus in Pregnancy, Pregnancy, High Risk
Keywords
Pregnancy, Gestational Diabetes, Screening, Maternal Outcomes, Neonatal Outcomes

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a prospective, single-center, randomized study evaluating an early screening protocol for identifying women at high risk for developing GDM to the routine standard of care for GDM screening.
Masking
Outcomes Assessor
Masking Description
Those assessing the outcomes from the medical chart will be blinded to the randomization process and the assigned study arm. Patients, the primary investigator, and their care providers will be aware of their treatment status.
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Enhanced First Trimester GDM Screening
Arm Type
Experimental
Arm Description
Women who are randomly assigned to this condition will be required to have early glucose screening with a prediction model composed of additional clinical risk factors and serum biomarkers (triglycerides, PAPP-A, and lipocalin-2) with their initial prenatal laboratory assessment.
Arm Title
Standard of Care GDM Screening
Arm Type
Active Comparator
Arm Description
Women who will be randomized to the comparison condition of usual standard of care will undergo routine standard of care. The standard of care will consist of routine screening for diabetes in pregnancy between 24 to 28 weeks of gestation via the two-step screening method with possible early screening with either plasma fasting glucose, oral glucose tolerance test, or hemoglobin A1c at the providers discretion to represent true clinical practice.
Intervention Type
Diagnostic Test
Intervention Name(s)
Enhanced First Trimester GDM Screening
Intervention Description
Women who are randomly assigned to this condition will be required to have early glucose screening with a prediction model composed of additional clinical risk factors and serum biomarkers (triglycerides, PAPP-A, and lipocalin-2) with their initial prenatal laboratory assessment.
Intervention Type
Diagnostic Test
Intervention Name(s)
Routine Gestational Diabetes Screening
Other Intervention Name(s)
Third Trimester Screening
Intervention Description
Women who will be randomized to the comparison condition of usual standard of care will undergo routine standard of care. The standard of care will consist of routine screening for diabetes in pregnancy between 24 to 28 weeks of gestation via the two-step screening method with possible early screening with either plasma fasting glucose, oral glucose tolerance test, or hemoglobin A1c at the providers discretion to represent true clinical practice.
Primary Outcome Measure Information:
Title
Gestational Diabetes Mellitus
Description
Confirmed diagnosis of GDM based on 3 hour 100 gram glucose tolerance test
Time Frame
In pregnancy (24-28 weeks gestation)
Secondary Outcome Measure Information:
Title
Mode of Delivery
Description
Mode of delivery (Vaginal versus Cesarean delivery)
Time Frame
At Birth
Title
Neonatal Birthweight
Description
Neonatal Birthweight
Time Frame
At Birth
Title
Number of Participants with Shoulder Dystocia
Description
Number of Participants with Shoulder Dystocia
Time Frame
At Birth
Title
Number of participants with brachial plexus injury
Description
Number of participants with brachial plexus injury
Time Frame
At Birth
Title
APGAR Score
Description
APGAR Score (range 0 to 10, with 10 being the best)
Time Frame
At Birth
Title
Neonatal Intensive Care Unit Admission
Description
Admission to Level 2 or greater neonatal ICU and length of stay
Time Frame
At delivery and within first 2 days of life
Title
Gestational Age at Delivery
Description
Gestational Age at Delivery
Time Frame
At Birth
Title
Patient Satisfaction with Diabetes Screening Method
Description
This will be assessed by the Patient Satisfaction Survey questionnaire, which is scored out of 30, with 30 being the highest score)
Time Frame
Postpartum day 1 after birth

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1) age greater than or equal to 18 years old, 2) singleton gestation less than or equal to 12 weeks at initial obstetric visit, 3) receiving prenatal care at UMMHC and plans to deliver at UMMHC, 4) able and willing to provide informed consent, 5) English or Spanish speaking, and 6) are at high risk for developing GDM by ACOG clinical risk factor guidelines. Exclusion Criteria: 1) known diagnosis of pre-existing pregestational diabetes, 2) plan to receive prenatal care or deliver outside of UMMHC, 3) inability to complete oral glucose tolerance test (e.g. gastric bypass surgery history, gastric dumping syndrome history, vomiting of oral glucose tolerance test), or 4) systemic steroid use.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gianna L Wilkie, MD
Phone
77743642523
Email
Gianna.Wilkie@umassmemorial.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gianna Wilkie, MD
Organizational Affiliation
University of Massachusetts Chan Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Massachusetts Memorial Medical Center
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01605
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29898442
Citation
Sweeting AN, Wong J, Appelblom H, Ross GP, Kouru H, Williams PF, Sairanen M, Hyett JA. A Novel Early Pregnancy Risk Prediction Model for Gestational Diabetes Mellitus. Fetal Diagn Ther. 2019;45(2):76-84. doi: 10.1159/000486853. Epub 2018 Jun 13.
Results Reference
result
PubMed Identifier
21268030
Citation
Nanda S, Savvidou M, Syngelaki A, Akolekar R, Nicolaides KH. Prediction of gestational diabetes mellitus by maternal factors and biomarkers at 11 to 13 weeks. Prenat Diagn. 2011 Feb;31(2):135-41. doi: 10.1002/pd.2636. Epub 2010 Dec 28.
Results Reference
result

Learn more about this trial

Early Detection of Gestational Diabetes Mellitus in Pregnancy

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