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临床试验/IRCT2015080722407N3
IRCT2015080722407N3已完成3 期

The effectiveness of acupressure on pain relief after cesarean.

Vice Chancellor for research; Shahroud University of Medical Sciences0 个研究点目标入组 108 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
发起方
入组人数
108

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 45 years(—)
性别
Female

入选标准

  • Having at least primary education level; full consciousness in women after cesarean section; no previous experience using acupressure for any reason; no injuries; without bruising, tenderness or itching on LI4 location; all repeated cesarean and cesarean patients, including those who are first cesarean. Exclusion criteria: Patients with pre-eclampsia in the postoperative period which magnesium sulfate have been used for them.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research; Shahroud University of Medical Sciences

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