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临床试验/NCT02332759
NCT02332759已完成不适用

A PILOT STUDY TO EVALUATE THE PRELIMINARY SAFETY AND FEASIBILITY OF THE MATERNA MEDICAL DEVICE FOR THE PREVENTION OF PERINEAL LACERATIONS AND OCCULT DISRUPTION OF THE PELVIC FLOOR AND ASSOCIATED SEQUELA DURING VAGINAL DELIVERY.

Baylor College of Medicine2 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2014年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
61
试验地点
2
主要终点
No adverse events related to device

研究概览

简要总结

The Materna device aims to prevent pelvic tissue damage by preventing overstretching of pelvic floor muscle fibers during delivery. The device is a single use, disposable, mechanical dilator that penetrates the first 4 cm or ½ of the vaginal canal and gradually expands the vagina from a resting diameter of 2-3 cm to the fully expanded size of a delivering fetus, roughly 8-10 cm. The Materna device will be used during the first stage of labor, for roughly 1-2 hours, in a hospital Labor and Delivery unit, under the supervision of trained clinical labor and delivery providers

详细描述

Over 80% of women who deliver vaginally will sustain a vaginal tear, and roughly half of all women will suffer from permanent pelvic muscle damage that may lead to pelvic disorders later in life.(1-8) The consequences of vaginal tearing are acute and chronic pain, longer recovery times, sexual dysfunction and permanent disfigurement.(1-4) Additionally, women often say that the prospect of tearing is one the things they fear most regarding childbirth. Tearing during childbirth is well documented as occurring during most deliveries, however there is additional damage now being discovered that occurs internally to the pelvic muscles.

It has long been thought that childbirth is the leading factor contributing to the development of pelvic floor disorders such as pelvic organ prolapse, urinary and fecal incontinence. (6,9,10) In the last 10 years, new imaging studies have shown that approximately 20-30% of women will have their pelvic muscles permanently separated from the pelvic bone during vaginal delivery.(5-11) In an additional 20-30% of cases, the muscles may remain attached to the pelvic bone but have been stretched to the point of becoming functionally compromised

One of the most promising ideas to prevent this damage is to slowly prepare the pelvic muscles, during labor while the cervix is dilating, in order to maximize their stretch.

The previous data and preliminary findings of Materna suggest the following overall working hypotheses:

  1. Vaginal lacerations and pelvic floor muscle damage lead to increased incidence of pelvic floor disorders and other negative sequelae.
  2. Vaginal lacerations and pelvic floor muscle damage are caused by over straining of pelvic muscles and vaginal tissues without maximizing the tissue strain using appropriate viscoelastic relaxation during the second phase of labor.
  3. The incidence and severity of vaginal lacerations and pelvic floor muscle damage can be reduced by inducing a more gradual strain of the vaginal tissues using a device-based approach

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Primiparas, or previous pregnancy terminated before 24 weeks gestation
  • Single fetus birth
  • Subject is able to understand the risks and potential benefits of participating in the study and is willing to provide written informed consent
  • Subject is willing and able to comply with specified follow-up evaluations
  • Planned to have epidural during birthing process

排除标准

  • Previous delivery, or previous pregnancy beyond 24 weeks gestation
  • Less than 36 weeks gestation
  • Neurological diseases e.g. Multiple Sclerosis that may result in unrelated pelvic disorders
  • Muscular or skin disorder that effects elasticity of tissue such as scleroderma or lupus
  • Local or systemic infection e.g. HIV, herpes
  • Clinically estimated fetal weight > 4,500 grams
  • Any prior surgical procedures to the vaginal anatomy which could lead to pelvic dysfunction, pelvic fractures, or pelvic soft tissue injuries. Evaluated during baseline screening
  • High likelihood of less than 1 hour of potential device dilation time after the woman arrives at the center and receives epidural
  • A cervical dilation of greater than or equal to 6 cm
  • BMI > 32.5 prior to becoming pregnant

结局指标

主要结局

No adverse events related to device

时间窗: 12-20 week postpartum follow up

次要结局

  • Reduction in perineal lacerations and pelvic floor trauma(12-20 week postpartum follow up)

研究者

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

Francisco Orejuela

Principal Investigator

Baylor College of Medicine

研究点 (2)

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