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临床试验/NCT02330471
NCT02330471已完成3 期

Forced Versus Spray Coagulation in Women Undergoing LLETZ-conization for Cervical Dysplasia: a Randomized Trial

Ruhr University of Bochum2 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2014年1月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
160
试验地点
2
主要终点
time to complete intraoperative hemostasis

研究概览

简要总结

In a randomized clinical trial of 120 women undergoing large loop excision of the transformation zone (LLETZ)-conization for cervical dysplasia, two coagulation modes, spray versus forced coagulation, will be compared. The primary outcome of the study is time to complete hemostasis, secondary outcomes are intraoperative blood loss, postoperative pain, and postoperative bleeding complications.

详细描述

Intraoperative bleeding during large loop excision of the transformation zone (LLETZ)-conization can be achieved by two modes of electrocoagulation, spray coagulation and forced coagulation. Spray coagulation is a superficial coagulation mode, whereas forced coagulation is a deep tissue coagulation mode. It is unknown, whether spray or forced coagulation is superior regarding intraoperative hemostasis and other outcome Parameters such as postoperative bleeding and postoperative pain. Therefore, the investigator designed a randomized clinical trial of 120 women undergoing large loop excision of the transformation zone (LLETZ)-conization for cervical dysplasia, comparing the two coagulation modes, spray coagulation and forced coagulation, The primary outcome of the study is time to complete hemostasis measured in seconds, secondary outcomes are intraoperative blood loss measured as difference in serum hemoglobin pre- and postoperatively, postoperative pain according to a 10 step VAS scale, and postoperative bleeding complications, defined as necessity to intervene surgically for vaginal bleeding up to 14 days postoperatively. The study Population consists of women undergoing LLETZ-conization for histologically proven cervical dysplasia. The study hypothesis states that the difference in the mean time until complete hemostais will be at least 1/3 shorter in women randomized to spray coagulation. With a study Population of 120 women, this study has a power of >80% to detect a difference of 1/3 of the mean coagulation time until complete hemostais based on an anticipated mean time of 85 seconds.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • histologically proven cervical dysplasia
  • colposcopy Prior to LLETZ-conization
  • informed consent
  • no known hematologic disorder

排除标准

  • significant language barrier
  • a personal history of LLETZ-conization

结局指标

主要结局

time to complete intraoperative hemostasis

时间窗: 120 seconds

the time until complete hemostasis as judged by the surgeon has been achieved, will be measured in seconds

次要结局

  • postoperative pain(5 hours)
  • postoperative complications(14 days)
  • intraoperative blood loss(5 hours)

研究者

发起方
Ruhr University of Bochum
申办方类型
Other
责任方
Principal Investigator
主要研究者

Clemens Tempfer

Clemens Tempfer, MD

Ruhr University of Bochum

研究点 (2)

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