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临床试验/NCT02248519
NCT02248519已完成不适用

Laparoscopic Versus Open Gastrectomy for Gastric Cancer, a Multicenter Prospectively Randomized Controlled Trial (LOGICA-trial)

UMC Utrecht10 个研究点 分布在 1 个国家目标入组 210 人开始时间: 2014年12月1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
UMC Utrecht
入组人数
210
试验地点
10
主要终点
Post-operative hospital stay

研究概览

简要总结

This is the first randomized controlled trial comparing laparoscopic and open gastrectomy for resectable gastric cancer in a Western population. The hypothesis is that laparoscopic gastrectomy will result in a lower post-operative burden by means of shorter post-operative hospital stay. Secondarily that laparoscopic gastrectomy is hypothesized to be associated with lower post-operative morbidity and readmissions, higher cost-effectiveness, and better post-operative quality of life, with similar mortality and oncologic outcomes, compared to open gastrectomy. The study starts on 1 December 2014. Inclusion and follow-up will take three and five years respectively. Short-term results will be analyzed and published after discharge of the last randomized patient.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically proven adenocarcinoma of the stomach
  • Surgically resectable (cT1-4a, N0-3b, M0) tumor
  • Age ≥ 18 years
  • European Clinical Oncology Group (ECOG) performance status 0, 1 or
  • Written informed consent

排除标准

  • Siewert type I esophagogastric junction tumor
  • Non-elective surgery
  • Previous gastric resection or recurrent gastric cancer
  • Pregnancy

研究组 & 干预措施

Open Gastrectomy

Active Comparator

Patients allocated to the 'Open Gastrectomy' group will receive distal or total gastrectomy via laparotomy. This group is considered the control group

干预措施: Open Gastrectomy (Procedure)

Laparoscopic Gastrectomy

Experimental

Patients allocated to the 'Laparoscopic Gastrectomy' group will undergo distal or total gastrectomy via laparoscopy.

干预措施: Laparoscopic Gastrectomy (Procedure)

结局指标

主要结局

Post-operative hospital stay

时间窗: During admission, an expected average of 2 weeks

The primary outcome of this study is the post-operative hospital stay (days), since this is considered a strong end point as it reflects the impact of the different surgical procedures.

次要结局

  • Mortality(30 days post-operative)
  • Post-operative morbidity(Up to 5 years post-operative)
  • Cost-effectiveness(Up to 5 years post-operative)
  • Quality of Life(Up to 5 years post-operative)
  • Readmissions(Up to 5 years post-operative)
  • Oncologic outcomes (R0-resection rate and lymph node yield)(Pathology report 1-2 weeks after surgery)

研究者

发起方
UMC Utrecht
申办方类型
Other
责任方
Principal Investigator
主要研究者

Richard van Hillegersberg

MD PhD

UMC Utrecht

研究点 (10)

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