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临床试验/NCT01531504
NCT01531504已完成不适用

Evaluation of Safety and Effectiveness of ViKY Device for Uterine Positioning

EndoControl4 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2011年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
EndoControl
入组人数
30
试验地点
4
主要终点
Effectiveness

研究概览

简要总结

Evaluation of Safety and Efficacy of ViKY Device for Uterus Positioning on 2 US sites

详细描述

The ViKY device "Vision Control for endoscopy" was initially a compact motorized endoscope holder for laparoscopic surgery. It holds the endoscope and is controlled by either a foot pedal or voice activation. It received FDA approval in December 2008 and since that time has been used to facilitate laparoscopic surgery in multiple specialties.

EndoControl now considers using the technology for uterus manipulation in laparoscopic-assisted hysterectomies. Most gynecologic surgeries require displacement of the uterus out of the anatomic location to optimize the surgery. During an abdominal hysterectomy clamps are placed on the uterine cornua allowing easy manipulation of the uterus. The development of laparoscopic surgery required new techniques to manipulate the uterus. Typically a uterine manipulator is placed vaginally and controlled by the surgeon or the surgical assistant during the procedure.

In conventional operations, the constant physical force decreases the surgical team's efficacy and increases fatigue levels. The use of the ViKY device to control the position of the uterus facilitates surgery by enabling the surgeon to maintain a constant "locked" position or by allowing the surgeon to remotely move the uterus at any point of the surgery. The ViKY device also eliminates the need for an extra surgical assistant during laparoscopic-assisted hysterectomies.

The aim of this study is to collect data to demonstrate safety and effectiveness of the use of the ViKY device for uterine manipulation during conventional laparoscopic-assisted hysterectomies or computer-controlled laparoscopic hysterectomies.

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Age 18-80
  • Candidate for conventional laparoscopic-assisted hysterectomies procedures
  • patient has a cervix and a uterus
  • Exclusion criteria
  • Difficulty understanding the English language
  • Anatomy that precludes the use of a uterine manipulator
  • Current inclusion in another research study

排除标准

  • 未提供

结局指标

主要结局

Effectiveness

时间窗: 4 months

Number of cases with adequate visualization of pelvic anatomy during endoscopy.

Adverse Events

时间窗: 4 months

Number of perforations during intervention. Number of complications associated with the use of uterine manipulator

次要结局

  • surgery characterization(4 months)

研究者

发起方
EndoControl
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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