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临床试验/IRCT2016072529063N1
IRCT2016072529063N1已完成未知

The survey effect of lavender aromatherapy on the pain level after cesarean section among women referred to Al-Zahra hospital in Rasht in 2016- 2017

Guilan university of Medical Sciences0 个研究点目标入组 110 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
发起方
入组人数
110

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
15 years 至 45 years(—)
性别
Female

入选标准

  • pain VAS score higher than 3; using spinal anesthesia; use of a type of anesthetic(bupivacaine 0.05); no concurrent operation; duration of operation less than 90 min; full term pregnancy; no history of allergies to medicinal plants, anosmia, migraines, chronic headaches, coagulation disorders, polyhydramnios, diabetes, preeclampsia, twin pregnancy.
  • Exclusion criteria: nausea, vomiting; allergy or absence of patients satisfaction after first dose of aromatherapy.

排除标准

  • 未提供

研究者

发起方
Guilan university of Medical Sciences

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