跳至主要内容
临床试验/NCT03326895
NCT03326895已完成不适用

A Prospective, Multi-Center Evaluation of the ECHELON CIRCULAR Powered Stapler in Left-Sided Colorectal Anastomoses

Ethicon Endo-Surgery22 个研究点 分布在 5 个国家目标入组 168 人开始时间: 2017年11月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
168
试验地点
22
主要终点
Percentage of Participants With Stapler Performance Issues

研究概览

简要总结

This prospective clinical study will evaluate the intra-operative performance of the powered circular stapler used in left colectomy procedures in a post-market setting.

详细描述

Surgical staplers have been utilized in colorectal procedures since the early 20th century, with intraluminal staplers used to create the anastomosis since 1979. Successful utilization of these devices, whether in open or laparoscopic procedures, requires extensive training and experience. Even with experience, device issues such as stapler misfire, incomplete firing, low surgeon satisfaction, etc., may occur. In a retrospective study of 349 colorectal resections, 67 (19%) procedures had some type of technical error. The most frequently reported issues from the analysis were positive leak tests, difficulty placing or removing the stapler, and inadequate donuts. Surgeons may also experience psychological or physical stress during procedures due to complications, workload, or other factors.

Patients scheduled to undergo a left-sided colon resection, and who meet study entry criteria, may be enrolled. Investigators will perform each procedure using the powered circular stapler according to the instructions for use (IFU). There will be no blinding or planned-interim analysis. Procedures may be performed open or via minimally invasive surgery (MIS) according to institutional standard-of-care (SOC). Use of a hand port and robotic assistance are permissible providing the powered circular stapler is used to create the anastomosis. Conversion from laparoscopic to open surgery is permissible under the protocol at the surgeon's discretion for the patient's safety.

The final scheduled study visit will occur 28 days post-procedure (routinely scheduled follow-up with surgeon). Follow-up by phone is permissible when an on-site visit is not planned or is more than six weeks post-operative.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Scheduled for colectomy with left-sided anastomosis peformed with a circular stapler;
  • Willing to give consent and comply with all study-related evaluations; and
  • At least 18 years of age.

排除标准

  • Enrollment in a concurrent clinical study;
  • Physical or psychological condition which would impair study participation;
  • Emergency surgery;
  • ASA Class ≥ IV;
  • The subject is judged unsuitable for study participation by the Investigator; or
  • Unable or unwilling to provide follow-up information 8, Undergoing multiple intraoperative synchronous colon resections;
  • Anastomosis not distal from splenic flexure of the colon
  • Anastomosis of the colon not attempted
  • Subjects with any intraoperative findings identified by the surgeon that would preclude attempting an anastomosis with a circular stapler.

结局指标

主要结局

Percentage of Participants With Stapler Performance Issues

时间窗: Intraoperative

A stapler performance issue is defined as a failure of the ECHELON CIRCULAR Powered Stapler to perform per its instructions for use. This includes but is not limited to difficulty placing or removing the stapler, stapler misfire/failure of the device to fully fire, staple line defects, incomplete or thin donuts, tissue damage, positive intraoperative leak test, detached components, unformed staples, or any other device failure.

次要结局

  • SURG-TLX Questionnaire(Collected postoperative for intraoperative stress)

研究者

发起方
Ethicon Endo-Surgery
申办方类型
Industry
责任方
Sponsor

研究点 (22)

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