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临床试验/NCT03944291
NCT03944291已完成3 期

Unilateral vs. Bilateral Pudendal Nerve Block for Post-Episiotomy Pain Relief: A Randomized Clinical Trial

Ain Shams University1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2019年5月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
102
试验地点
1
主要终点
Visual Analogue Scale for pain scoring

研究概览

简要总结

Unilateral vs. Bilateral Pudendal Nerve Block for Post-Episiotomy Pain Relief: A Randomized Clinical Trial

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Term (37 to 42 weeks gestation), primigravid women with singleton vertex fetus

排除标准

  • Women with bleeding disorders, known hypersensitivity to local anesthetics, chronic use of pain medication, had previous vaginal surgery, extensive vulvovaginal infection, malposition or malpresentation were excluded from the study. Also, women who failed to deliver vaginally, had extensive perineal or cervicat tears, or had instrumental delivery were excluded from the final analysis of the study

结局指标

主要结局

Visual Analogue Scale for pain scoring

时间窗: 48 hours

visual analogue scale (VAS) from 0 to 100 with 0 corresponding to no pain at all and 100 as the worst pain the woman can describe

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohamed S Sweed, MD

Principal Investigator

Ain Shams University

研究点 (1)

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