跳至主要内容
临床试验/TCTR20200924002
TCTR20200924002尚未招募3 期

Midline incisional hernia prophylaxis using synthetic mesh in emergency or urgency gastrointestinal tract surgery: A multicenter randomized clinical trial

Vajira Hospital, Navamindradhiraj University0 个研究点目标入组 470 人开始时间: 2020年9月24日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
470

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 0 N/A (No limit)(—)
性别
All

入选标准

  • 1. Adults age ≥ 18 years
  • 2. Surgery within 24 hours after admission or consultation with suspected GI pathology
  • 3. Receipt of midline abdominal incision with an incision length of at least 1/4 of the distance from the xiphoid process to the pubic symphysis
  • 4. Have an American Society of Anesthesiologist (ASA) physical status class 1-4

排除标准

  • 1. Any of following conditions:
  • 1.1. Septic shock (hemodynamic instability)
  • 1.2. Metastatic cancer (stage IV) at before or during operation
  • 1.3. Dirty surgical wound with severe contamination from fecal material and frank pus (surgical wound class IV)
  • 1.4. Massive devitalized bowel ischemia
  • 2. potential second-look operation or planned revisionary surgery via a midline incision
  • 3. secondary fascial closure
  • 4. existence of midline incisional hernia and/or history of midline incisional hernia repair
  • 5. pregnancy or plan for pregnancy after surgery
  • 6. connective tissue disorders
  • 7. current or planned immunosuppressive use
  • 8. allergy to polypropylene

研究者

发起方
Vajira Hospital, Navamindradhiraj University

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