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临床试验/NCT01533467
NCT01533467已完成2 期

Study of Perineal Protection Device

Helsingborgs Hospital2 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2010年11月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
1,200
试验地点
2
主要终点
Grade I and II rupture during delivery

研究概览

简要总结

Objective:

To investigate the protective effects of a newly invented device for reducing tears in the perineum during vaginal childbirth.

Design:

A multicenter randomized control trial performed at three hospitals in Sweden, in Helsingborg, Lund and Malmö. Participants recruited are women with vaginal delivery (N=1200), cephalic presentation. They will be randomized to an intervention group, with a perineal protection device, and a control group deliver as normal.

Main outcome measures:

The effect on the frequency and extension of perineal ruptures grade I, II and anal sphincter rupture are measured.

详细描述

Perineal rupture shall be measured with a ruler. Anal sphincter ruptures be examined by physicians. Drawing be made of the tears by the midwife.

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
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Vaginal delivery

排除标准

  • Age below 18 years and no understanding of written and oral information.

结局指标

主要结局

Grade I and II rupture during delivery

时间窗: time at the delivery department (up to 12 months)

Number and extension of perineal tears during delivery

次要结局

未报告次要终点

研究者

发起方
Helsingborgs Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Knut Haadem

Principal investigator

Helsingborgs Hospital

研究点 (2)

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