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临床试验/TCTR20230605004
TCTR20230605004招募中2 期

Efficacy of intravenous glucose-contained fluid in reducing labor duration of pregnant women : A randomized controlled trial

Department of Obstetrics and Gynecology, Sunpasitthiprasong hospital0 个研究点目标入组 160 人开始时间: 2023年6月5日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
160

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
Female

入选标准

  • 1) Single fetal pregnancy which the women age between 18-45 years, and presenting with labor pain at Sunpasitthiprasong hospital.
  • 2) Gestational age between 37 weeks 0 day to 41 weeks 6 days
  • 3) The pregnant women has uterine contraction with cervical so opening between 3-5 cm.

排除标准

  • 1) The pregnant women do not want to be the participant.
  • 2) High risk pregnancy, for example
  • - Gestational diabetes mellitus, Overt diabetes mellitus
  • - All type of heart disease
  • - All type of renal disease
  • - All type of liver disease
  • - Pregnancy-induced hypertension, Pre-eclampsia
  • 3) Contraindications for vaginal delivery
  • - Abnormal fetal presentation, for example, breech and transverse presentation.
  • - Fetal macrosomia (definition by estimated fetal weight beyond 4,000 grams)
  • - Inadequated pelvis or Cephalopelvic disproportion.
  • - All type of abnormal placentation, for example, placenta previa or placenta adheren
  • - Previous cesarean section.
  • - History of previous ectopic pregnancy at cornu area, and receive treatment by surgical wedge resection.
  • - Myoma or structural uterine abnormalities that prevent vaginal delivery.
  • 4) Fetal abnormalities, for example, Non-reassuring fetal status, fetal anomalies, and death fetus in utero.

研究者

发起方
Department of Obstetrics and Gynecology, Sunpasitthiprasong hospital

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