IRCT201504236582N10已完成未知
Comparison the efficacy of lavender aroma and valerian in reducing labor pain and Progress of labor in nulliparous women
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 141
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
- •Inclusion Criteria: Primiparous pregnancy; age 18-35; gestational age of 37-41 w; singleton fetus; active phase; cephalic presentation; no smoking; no addiction; no Lack of vision; no history of chronic heart diseases, lung diseases, according to the patient's expression; the absence of eclampsia; and placenta previa; no PROM for more than 18 hours; no history of infertility; willingness to participate in the study; no history of sensitivity; the presence of low-risk pregnancies.
排除标准
- •Get analgesic medication during the 3 hours before the start of the study; systolic blood pressure less than 95 mm Hg.
研究者
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