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临床试验/IRCT20230301057585N1
IRCT20230301057585N1尚未招募3 期

Comparison of the effect of lavender and clove essential oil on the intensity of pain and anxiety of the first stage of labor

Gonabad University of Medical Sciences0 个研究点目标入组 159 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
159

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

  • Women with first and second pregnancy, aged 18-35 years, pregnant with single fetus , having a normal delivery, 38-42 weeks of pregnancy, cephalic presentation, cervical dilatation more than 3 cm.
  • No history of asthma, sensitivity and allergy according to mother's statements.
  • Absence of disease and complications of pregnancy and obstetrics (such as: pre-eclampsia - chorioamnionitis - known liver, gallbladder and respiratory disease, decollement and abnormal heartbeat of the fetus at the beginning of the study),
  • Not having smell problems and allergies to herbal medicines according to the person.
  • Not having a known anxiety and depression disease according to the person's statements in the medical history and the mother's file.
  • Not having migraines according to the mother's statements in the medical history.
  • Not receiving medical painkillers 3 hours before the start of the study.
  • There is no history of infertility and thyroid disease according to the person's statements in the medical history and the mother's file.
  • Informed consent of women to participate in the study

排除标准

  • Mother's non-cooperation in completing the checklist and expressing her pain
  • Departure from the natural course of labor
  • Having an emergency caesarean section
  • Allergic to essential oil
  • Fetal weight less than 2.5 kg or more than 4 kg

研究者

发起方
Gonabad University of Medical Sciences

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