跳至主要内容
临床试验/IRCT138812193527N1
IRCT138812193527N1已完成未知

The Study of Effect of Acupressure in SP6 on Labor Pain and Labor Outcome in Women During Labor

Tarbiat Modares University0 个研究点目标入组 131 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
131

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 35 years(—)
性别
Female

入选标准

  • 18 to 35 years-old pregnant women; 38-42 weeks gestational age; parity of 1 or 2; no use of psycho-therapeutics nor labor induction medications prescribed by physician or midwife; no use of chemical or natural pain killers prior to the study; cervical dilatation of 3-5cm; BMI less than 29; devoid of any medical or obstetrical problems such as uterine myomas, pre-cancerous lesions, cephalopelvic disproportion, infertility or surgical operation on uterus or cervix, placenta previa, placental abruption, poly- or oligohydramnios, erythroblastosis fetalis, preeclampsia, gestational diabetes, decreased fetal movements; no use of tobacco (e.g., smoking, hubble bubble, drugs) or alcohol and no verbal, auditory, or mental problems.
  • Exclusion criteria: lack of consent;
  • oxytocin dose in excess of routine requirements and any sign of fetal distress such as a heart rate of over 160 or less than 110beats/min, late decelerations, thick meconium staining and prolonged or precipitate labor, newborn weighing less than 2500 or more than 4000 grams

排除标准

  • 未提供

研究者

相似试验