跳至主要内容
临床试验/NCT07034261
NCT07034261尚未招募不适用

Continuous Glucose Monitoring to Detect Postpartum Dysglycemia in Patients With Gestational Diabetes

University of Chicago0 个研究点目标入组 50 人开始时间: 2026年9月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
主要终点
Determine the ability of continuous glucose monitoring to predict dysglycemia

研究概览

简要总结

The aim of this study is to determine the ability of postpartum continuous glucose monitoring (CGM) for subjects with gestational diabetes (GDM) to predict dysglycemia on 4-12 week postpartum oral glucose tolerance test (OGTT).

详细描述

Gestational diabetes (GDM) is glucose intolerance that develops during pregnancy. In the US, GDM affected 8.3% of pregnancies in 2021. Persistent glucose intolerance is present in up to 20% of women at post-partum follow up and subsequent risk for type 2 diabetes is significantly increased. All patients with GDM should undergo post-partum oral glucose tolerance test (OGTT) at 4-12 weeks to identify persistence glucose intolerance or overt diabetes. Detecting postpartum dysglycemia in people with GDM is a critical step for reducing long-term risk of type 2 diabetes and its associated complications. However, <50% of people complete the postpartum OGTT due to barriers in transportation, finances, and childcare. Recent studies have examined the use of postpartum continuous glucose monitoring (CGM) and proposed CGM metrics to predict dysglycemia on postpartum OGTT in people with GDM. These findings should be validated in other cohorts to confirm broad applicability.

This pilot study aims to enroll subjects with GDM at the University of Chicago to wear a blinded CGM for 14 days postpartum (study intervention) and then complete a OGTT at 4-12 weeks postpartum (standard of care).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Age greater than or equal to 18
  • Completed pregnancy with delivery of a live born infant(s). Pregnancies with multiple gestations will be included
  • No prior history of type 1 or type 2 diabetes
  • * Patients with a history of gestational diabetes (GDM) in a prior pregnancy will be eligible for inclusion.
  • GDM diagnosis by standard screening at 24-28 weeks
  • 2 hour 75g oral glucose tolerance test (OGTT); one abnormal value required for diagnosis
  • Fasting glucose 92
  • 1 hour 180
  • 2 hour 153
  • 3 hour 100g OGTT - two abnormal values required for diagnosis
  • Fasting glucose - 95
  • 1 hour 180
  • 2 hour 155
  • 3 hour 140
  • There are no

排除标准

  • for this study. Eligibility will be based on inclusion criteria.

研究组 & 干预措施

Blinded Continuous Glucose Monitoring Device

Experimental

Subjects will wear a blinded continuous glucose monitoring device.

干预措施: Blinded Continuous Glucose Monitoring Device (Device)

结局指标

主要结局

Determine the ability of continuous glucose monitoring to predict dysglycemia

时间窗: baseline to Day 70

Assess the validity of the continuous glucose monitoring metrics (percentage) proposed by Cabrera et al. (percent time \>180 of \>4%)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

相似试验