IRCT20180903040936N1尚未招募2 期
Comparison of efficacy of painless delivery with epidural analgesia with Bupivacain and Rupivacain in womwn candidating Analgesia labor
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 入组人数
- 112
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
- no limit 至 no limit（—）
- 性别
- Female
入选标准
- •Mothers with one fetus
- •Pregnant mothers who are candidates for vaginal delivery (Physiological delivery)
- •Nullipar pregnant mothers are candidates for vaginal delivery
- •Pregnant women referring to Taleghani Hospital with informed consent to participate in the study.
- •Mothers with ASA grade one and two
- •Pregnant mothers between the weeks 37-42 Who are perfectly pregnant
- •Pregnant mothers who are candidates for vaginal delivery, who are satisfied with epidertal analgesia
排除标准
- •Patients in the epidural group who undergo epidural block failure after an epidural analgesia.
- •Pregnant mothers who are candidates for cesarean section for emergency reasons (such as placental abruption, umbilical cord prolapse, etc.).
研究者
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