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Treating Prediabetes in the First Trimester

Primary Purpose

Prediabetes, Gestational Diabetes

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Treatment of Prediabetes
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prediabetes focused on measuring First trimester treatment of prediabetes, First trimester treatment of gestational diabetes, Umbilical cord C-Peptide, Neonatal fat mass, Gestational weight gain, Infant obesity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Pregnant women age 18 and above
  • Any ethnic background
  • English- or Spanish-speaking
  • Planned prenatal care/delivery at The University of California, San Diego's Hillcrest Hospital
  • Singleton pregnancy
  • Prediabetes diagnosed prior to 15w0d with HbA1c 5.7-6.4% or FPG 92-125 mg/dL

Exclusion Criteria:

  • Known Type 2 Diabetes (T2DM)
  • T2DM diagnosed with first trimester screening
  • Patients with known maternal/fetal indications for delivery <36w0d
  • Patients presenting for care after 15w0d

Sites / Locations

  • UC San Diego Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

First Trimester Treatment of Prediabetes

Third Trimester Treatment of Prediabetes

Arm Description

Patients randomized to first trimester treatment will receive the following intervention immediately initiated upon diagnosis of prediabetes at <15 weeks 0 days gestation diabetes education blood glucose monitoring medications as needed per California Diabetes and Pregnancy established protocol growth ultrasounds antenatal testing

Patients randomized to third trimester treatment will receive the following intervention to be initiated at 28 weeks of gestation diabetes education blood glucose monitoring medications as needed per California Diabetes and Pregnancy established protocol growth ultrasounds antenatal testing

Outcomes

Primary Outcome Measures

Umbilical Cord C-Peptide >90th percentile

Secondary Outcome Measures

Neonatal fat mass
Neonatal fat mass will be measured using an anthropometric model using weight, length, and flank skinfold thickness.
Adherence to the Institute of Medicine (IOM) guidelines for gestational weight gain
The IOM recommends that underweight women (BMI<18.5kg/m2) gain 28-40lbs, normal women (BMI 18.5-24.9 kg/m2) gain 25-35lbs, overweight women (BMI 25.0-29.9 kg/m2) gain 15-25lbs and obese women (BMI≥30 kg/m2) gain 11-20 lbs.
Return to prepregnancy weight

Full Information

First Posted
August 15, 2013
Last Updated
October 9, 2018
Sponsor
University of California, San Diego
Collaborators
American College of Obstetricians and Gynecologists, Society for Maternal-Fetal Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT01926457
Brief Title
Treating Prediabetes in the First Trimester
Official Title
Treating Prediabetes in the First Trimester: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 15, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego
Collaborators
American College of Obstetricians and Gynecologists, Society for Maternal-Fetal Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators plan to study a sample of women with prediabetes (diagnosed by Hemoglobin A1c (HbA1c) 5.7-6.4% or fasting plasma glucose (FPG) 92-125 mg/dL) in the first trimester of pregnancy, and patients will be randomized to first trimester or third trimester treatment; the first trimester group will receive intervention immediately upon diagnosis of prediabetes whereas the third trimester group will receive only routine prenatal care until 28 weeks at which time they will receive intervention. Intervention is defined as: diabetes education blood glucose monitoring medications as needed growth ultrasounds antenatal testing The primary outcome is umbilical cord C-Peptide >90th percentile. Secondary outcomes include neonatal fat mass at delivery, infant weight-for-length at 12 months of age, maternal gestational weight gain, and biomarkers (chemicals) measured in the placenta and the baby's umbilical cord blood. The investigators hypothesize that women who undergo the above intervention in the first trimester will deliver significantly fewer neonates with umbilical cord C-Peptide >90th percentile, and that the neonates will have lower fat mass, and weight-for-length at 12 months. The investigators further hypothesize that a greater proportion of patients undergoing first trimester intervention will have appropriate maternal gestational weight gain as defined by the Institute of Medicine, and a greater proportion will return to prepregnancy weight within 12 months.
Detailed Description
The primary aim of the proposed research is to demonstrate that promoting a normoglycemic intrauterine milieu in women with prediabetes diagnosed in the first trimester of pregnancy with a Hemoglobin A1c (HbA1c) 5.7-6.4% or fasting plasma glucose (FPG) 92-125 mg/dL will decrease the accumulation of fetal white adipose tissue and development of infant/child obesity during the first year of life. This project is built upon the hypothesis that pregnant subjects with prediabetes randomized in the first trimester of pregnancy to strict glycemic control and pharmacotherapy as needed will have less fetal adiposity and adverse neonatal outcomes than those who receive the diagnosis of prediabetes but do not initiate care until the third trimester. In the proposed study, 240 women meeting the above criteria for prediabetes at ≤ 15w0d gestation will be randomized to either first trimester or third trimester treatment. Each group will have diabetes education, initiate blood glucose monitoring, begin pharmacotherapy as needed (per established protocol), undergo growth ultrasounds, and antenatal testing. The first trimester arm will receive the above interventions immediately upon diagnosis of prediabetes whereas the third trimester arm will receive only routine prenatal care until 28 weeks at which time they will begin education and treatment. Both groups will be treated identically from 28 weeks until delivery. In the 2013 the National Institutes of Health (NIH) Gestational Diabetes (GDM) Consensus Conference, the panel was concerned about adopting criteria that would increase prevalence of GDM (i.e. first trimester treatment) without first demonstrating improved outcomes. The results of this proposed trial, will allow us to fill key research gaps; this is the first prospective trial to evaluate the International Associations of Diabetes in Pregnancy Study Groups (IADPSG) recommendations for screening and diagnosing prediabetes in the first trimester. Findings from this research will quantify the maternal and neonatal benefits and harms of treating women with prediabetes from early pregnancy. Additionally, the cohort of neonates that will result from this study can be followed into childhood to evaluate whether first trimester treatment has benefits beyond those anticipated at birth and may decrease the long-term incidence of obesity and diabetes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetes, Gestational Diabetes
Keywords
First trimester treatment of prediabetes, First trimester treatment of gestational diabetes, Umbilical cord C-Peptide, Neonatal fat mass, Gestational weight gain, Infant obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
202 (Actual)

8. Arms, Groups, and Interventions

Arm Title
First Trimester Treatment of Prediabetes
Arm Type
Experimental
Arm Description
Patients randomized to first trimester treatment will receive the following intervention immediately initiated upon diagnosis of prediabetes at <15 weeks 0 days gestation diabetes education blood glucose monitoring medications as needed per California Diabetes and Pregnancy established protocol growth ultrasounds antenatal testing
Arm Title
Third Trimester Treatment of Prediabetes
Arm Type
Active Comparator
Arm Description
Patients randomized to third trimester treatment will receive the following intervention to be initiated at 28 weeks of gestation diabetes education blood glucose monitoring medications as needed per California Diabetes and Pregnancy established protocol growth ultrasounds antenatal testing
Intervention Type
Other
Intervention Name(s)
Treatment of Prediabetes
Intervention Description
Standardized treatment of prediabetes per California Diabetes and Pregnancy Program "Sweet Success" diabetes education blood glucose monitoring medications as needed per California Diabetes and Pregnancy established protocol growth ultrasounds antenatal testing
Primary Outcome Measure Information:
Title
Umbilical Cord C-Peptide >90th percentile
Time Frame
1 day (Collected at the time of delivery)
Secondary Outcome Measure Information:
Title
Neonatal fat mass
Description
Neonatal fat mass will be measured using an anthropometric model using weight, length, and flank skinfold thickness.
Time Frame
Within 48 hours of delivery
Title
Adherence to the Institute of Medicine (IOM) guidelines for gestational weight gain
Description
The IOM recommends that underweight women (BMI<18.5kg/m2) gain 28-40lbs, normal women (BMI 18.5-24.9 kg/m2) gain 25-35lbs, overweight women (BMI 25.0-29.9 kg/m2) gain 15-25lbs and obese women (BMI≥30 kg/m2) gain 11-20 lbs.
Time Frame
Weight gain will be measured from immediately preconception until delivery
Title
Return to prepregnancy weight
Time Frame
After 1 year post delivery
Other Pre-specified Outcome Measures:
Title
birthweight
Time Frame
At delivery
Title
birthweight percentile
Time Frame
At delivery
Title
Infant gender
Time Frame
At delivery
Title
Ponderal index
Description
Weight/length^3
Time Frame
At delivery
Title
Neonatal Intensive Care Unit (NICU) Admission
Time Frame
Within 10 days after birth
Title
Infant weight-for-length
Time Frame
6 months and 12 months after delivery
Title
Need for pharmacotherapy to control hyperglycemia
Time Frame
From 5 weeks gestation until time of delivery
Title
Birth trauma
Description
Shoulder dystocia, brachial plexus injury
Time Frame
At delivery
Title
Mode of delivery
Description
Spontaneous delivery, operative vaginal delivery, cesarean delivery
Time Frame
At delivery
Title
Indication for delivery
Time Frame
At delivery
Title
Total gestational weight gain
Time Frame
From immediately preconception until delivery
Title
Postpartum weight retention
Time Frame
Within 1 year of delivery
Title
Diagnosis of Preeclampsia
Time Frame
From 20 weeks gestation until 6 weeks postpartum

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Pregnant women age 18 and above Any ethnic background English- or Spanish-speaking Planned prenatal care/delivery at The University of California, San Diego's Hillcrest Hospital Singleton pregnancy Prediabetes diagnosed prior to 15w0d with HbA1c 5.7-6.4% or FPG 92-125 mg/dL Exclusion Criteria: Known Type 2 Diabetes (T2DM) T2DM diagnosed with first trimester screening Patients with known maternal/fetal indications for delivery <36w0d Patients presenting for care after 15w0d
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hilary A Roeder, MD
Organizational Affiliation
UC San Diego Health System
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gladys A Ramos, MD
Organizational Affiliation
UC San Diego Health System
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thomas R Moore, MD
Organizational Affiliation
UC San Diego Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC San Diego Health System
City
San Diego
State/Province
California
ZIP/Postal Code
92103
Country
United States

12. IPD Sharing Statement

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Citation
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Links:
URL
http://www.aaogf.org/
Description
The American Association of Obstetricians and Gynecologists Foundation
URL
https://www.smfm.org/about%20smfm%20foundation%20page.cfm?ht=s
Description
The Society For Maternal-Fetal Medicine Pregnancy Foundation
URL
http://repromed.ucsd.edu/
Description
UC San Diego Health System Department of Reproductive Medicine

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Treating Prediabetes in the First Trimester

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