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临床试验/IRCT2015062222874N1
IRCT2015062222874N1已完成3 期

Effects of entonox in comparison with lidocaine on severity of pain after episiotomy in nulliparous women

Ahvaz University of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
120

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
17 years 至 34 years(—)
性别
Female

入选标准

  • ( primi para women between 39 to 42 weeks of gestation according to sonography findings or last menstrual period date; mother’s age in 18 to 35 years; singleton; nulliparous; cephalic presentation; first trimester body mass index in range of 19.8 to 30 Kilograms per square meter. Exclusion criteria: presence of systemic diseases; abruption; post partume bleeding; sensitivity to local anesthesia or entonox).

排除标准

  • 未提供

研究者

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