跳至主要内容
临床试验/RBR-84xprt
RBR-84xprt进行中(未招募)1 期

Review of non-pharmacological interventions for pain relief in labor

Real e Benemérita Associação Portuguesa de Beneficência /SP0 个研究点开始时间: 2015年3月9日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Intervention

入排标准

年龄范围
18Y 至 55Y(—)
性别
Female

入选标准

  • Voluntary without any clinical or obstetric disease; active phase of labor with efficient two or three in ten minutes uterine contractions and cervical dilatation minimum 3 cm; gestational age between 37 completed weeks to complete 42 weeks calculated by last menstrual period or the result of early ultrasound until the twentieth week of pregnancy; minimum age of 18 years old and maximum age of 55 years; pregnancy with single live fetus in cephalic presentation bent; Note greatest pain 5 on the pain scale

排除标准

  • Volunteers with indication of caesarean section at admission; use of anesthesia during labor; Tobacco use less than two hours; people with mental disorders that may affect their autonomy; have ingested caffeine in the last 10 hours; use psychoactive drugs; performed less than 06 prenatal visits; use of natural or synthetic corticosteroids; used analgesics least at least 6 hours

研究者

发起方
Real e Benemérita Associação Portuguesa de Beneficência /SP

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