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临床试验/TCTR20260710003
TCTR20260710003进行中(未招募)不适用

Comparison of the Effects of Epidural Analgesia during Labor on Maternal Blood Glucose, Cortisol Levels, and Neonatal Outcomes in Parturients With or Without Gestational Diabetes Mellitus

未提供0 个研究点目标入组 126 人开始时间: 2026年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
126

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 40 Years(—)
性别
Female

入选标准

  • 1.Pregnant women aged 18 to 40 years
  • 2.Singleton pregnancy, cephalic presentation
  • 3.Gestational age 37 to 42 weeks, planned for vaginal delivery
  • 4.Cervical dilation 3 to 4 centimeters at the time of epidural catheter placement
  • 5.American Society of Anesthesiologists (ASA) physical status I to II, with no major underlying medical illness
  • 6.Willing and consenting to receive epidural labor analgesia
  • 7.For the gestational diabetes group: diagnosed with gestational diabetes mellitus according to the Vietnam Ministry of Health guideline (Decision 1470/QD-BYT, 2024), based on the 75 gram, 2 hour oral glucose tolerance test, managed by diet and exercise only, without insulin treatment
  • 8.For the comparison group: negative result on the above oral glucose tolerance test performed during the same period of pregnancy

排除标准

  • 1.Pre-existing type 1 or type 2 diabetes diagnosed before pregnancy
  • 2.Gestational diabetes mellitus requiring insulin treatment
  • 3.Endocrine disorders affecting cortisol or glucose metabolism, such as Cushing syndrome or adrenal insufficiency
  • 4.Severe preeclampsia, eclampsia, complete placenta previa, prior uterine scar, or threatened uterine rupture
  • 5.Fetal growth restriction, severe polyhydramnios, or severe oligohydramnios
  • 6.Current use of systemic corticosteroids, or last dose taken less than 72 hours before the onset of labor
  • 7.Contraindication to epidural analgesia, or refusal of the procedure by the patient

研究者

发起方
未提供

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