跳至主要内容
临床试验/NCT03374189
NCT03374189已完成不适用

Single Blind Randomized Control Trial Evaluating Efficacy and Safety of EZ-Close Port-site Closure Device Versus Carter-Thomason Device

Saint Vincent's Hospital, Korea2 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2017年8月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
79
试验地点
2
主要终点
Time Taken to Complete Closure

研究概览

简要总结

This study aims to evaluate the efficacy and safety of a novel port-site closure device (EZ Close) by comparing it with the Carter-Thomason device.

详细描述

Port-site closure is a critical procedure after every laparoscopic surgery. Complications such as visceral organ injury, port-site hernia, infection, ascitic fluid leakage may occur during and after the procedure. Many devices were developed and utilized for the procedure and Carter-Thomason is one of the most commonly used device and validated with several studies. This study aims to evaluate the efficacy and safety of a novel port-site closure device (EZ Close) by comparing it with the Carter-Thomason device.

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
Single (Participant)

入排标准

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

入选标准

  • All patients with laparoscopic ports over 10mm

排除标准

  • Patients with laparoscopic ports under 10mm
  • Patients who refused the study
  • Patients who received concurrent surgery for other reason

研究组 & 干预措施

EZ Close arm

Experimental

EZ close used for port-site closure.

干预措施: EZ close (Device)

Carter Thomason arm

Active Comparator

Carter Thomason used for port-site closure.

干预措施: Carter Thomason (Device)

结局指标

主要结局

Time Taken to Complete Closure

时间窗: At the time of surgery

The start of the procedure was defined as the point when the device was first inserted through the port-site and the end of the procedure was defined as the point when the port-site was removed from the port-site. A stopwatch was used to measure the time.

次要结局

  • Number of Participants With Visceral Organ Injury(At the time of surgery)
  • Number of Participants With Need for Additional Instrument(At the time of surgery)
  • Number of Participants With Port-site Hernia(3 days post-op and within one months of surgery)
  • Number of Participants With Port-site Infection(3 days post-op and within one months of surgery)
  • Number of Participants With Ascitic Fluid Leakage(3 days post-op and within one months of surgery)
  • Number of Participants With Wound Dehiscence(3 days post-op and within one months of surgery)

研究者

发起方
Saint Vincent's Hospital, Korea
申办方类型
Other
责任方
Principal Investigator
主要研究者

Hee Youn Kim

Assistant Professor

Saint Vincent's Hospital, Korea

研究点 (2)

Loading locations...

相似试验