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临床试验/ACTRN12610000529044
ACTRN12610000529044招募中不适用

A randomized, controlled trial of effects of low and high-frequency transcutaneous electric nerve stimulation (TENS) in Post Episiotomy Pain Relief.

niversity of Pernambuco0 个研究点目标入组 36 人开始时间: 2010年6月30日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
36

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
15 Years 至 o limit(—)
性别
Female

入选标准

  • Low risk pregnancy primiparous, older than 15 years old, literate, understanding the Portuguese Language, aware of time and space, post-natural childbirth, submitted to episiotomy with stitches, presenting pain in the episiotomy, and absence of any genitourinary pathology.

排除标准

  • TENS counter-indications as open wounds, presenting intolerance, irritation or great discomfort on the location where TENS was applied, puerperal relapse or recurrence (increased bleeding requiring intervention, phlogistic signs suggesting infection, fever, anesthesia complications, hypertension, mammary relapse or recurrences, morbid obesity (body weight 100 lb over the ideal weight).

研究者

发起方
niversity of Pernambuco

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