跳至主要内容
临床试验/NCT01241617
NCT01241617终止不适用

Randomized Trial Between Buttressed and Non Buttressed Stapling in Pulmonary Lobectomy

Medtronic - MITG1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2010年8月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
100
试验地点
1
主要终点
Frequency of intraoperative air leak

研究概览

简要总结

The objective of this study is to confirm superiority between a test treatment group using Endo GIA stapler with Duet Tissue Reinforcement System (TRS) and a current international standard of care group using a conventional stapler in patients undergoing pulmonary lobectomy surgery, using a randomized comparative study of the frequency of intraoperative air leak.

详细描述

Air leak is a complication of pulmonary surgical procedures that include pulmonary lobectomy, segmentectomy, and bullectomy, reported to occur in 33% to 75% of cases.

Prolonged air leak continuing for more than 7 days is reported to have a prevalence of greater than 15%. The presence of a history of smoking, preoperative steroid use, emphysema, low pulmonary function, pleural adhesion, and apical lung wedge resection are shown to be risk factors for prolonged air leak which lengthens the duration of drain placement, increases the days of hospitalization, and reduces patient ADL and QOL. Prolonged air leak may also result in serious complications, such as empyema.

Tissue reinforcement materials widely used as a pleural reinforcement to prevent air leaks during lung surgery, and are reported as a safe and effective material for body tissue reinforcement. Covidien Japan Inc. has developed a surgical stapler (Endo GIA Duet TRS) with an attached reinforcement material. This study will investigate the reinforcement effect on the staple line of using the newly developed surgical stapler with an attached reinforcement material.

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
Single (Participant)

入排标准

年龄范围
20 Years 至 79 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The patient is between 20-79 years of age.
  • The patient is eligible to be given pulmonary Lobectomy.
  • The patient is scheduled to undergo pulmonary Lobectomy.
  • Performance status 0~1 (Eastern Cooperative Oncology Group classification).
  • The patient has no history of lung surgery.
  • The patient is healthy organ function.
  • The patient is scheduled for surgery with staplers .
  • The patient must be willing and able to participate in the study procedures and able to understand and sign the informed consent.

排除标准

  • The patient has suffered thoracic trauma or has previously undergone pneumonectomy surgery.
  • The patient has an active bacterial infection or fungal infection.
  • The patient is undergoing continuing systemic administration (intravenous or oral) of steroids.
  • The patient condition is complicated by uncontrolled diabetes mellitus.
  • The patient participation is judged difficult due to study complications related to a psychiatric disorder or psychological symptoms.
  • The patient undergoes surgical procedure other than lobectomy during surgery.
  • Reinforcement material other than the study materials are applied during surgery.
  • The patient judged unsuitable for study participation by the investigator for any other reason.

结局指标

主要结局

Frequency of intraoperative air leak

时间窗: Day 0

Occurence of intraoperative air leak will vary from patient to patient and will be recorded for all patients.

次要结局

  • Postoperative duration of air leak(Month 1 (Average time period))
  • Duration of chest drainage(Month 1 (Average time period))
  • Frequency of intraoperative sealant use(Day 0)
  • Incidence of intraoperative adverse events(Day 0)
  • Incidence of postoperative adverse events(Month 1 (Average time period))
  • Days of hospitalization(Month 1 (Average time period))

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验