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临床试验/NCT03033719
NCT03033719Unknown不适用

Multicenter Randomized Trial Comparing Laparoscopy and Laparotomy for Colon Cancer Surgery in Patients Older Than 75 Years

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 276 人开始时间: 2017年7月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
276
试验地点
2
主要终点
Global postoperative morbidity in both arms

研究概览

简要总结

The purpose of this study is to compare the postoperative global morbidity between patients who have been operated on for a colon cancer by laparotomy and those operated on by laparoscopy

详细描述

The present study is a national, multicenter, open-label randomized, 2-arm superiority trial. Patients aged 75 years or older with uncomplicated colonic cancer or precancerous colonic lesion non-endoscopically resectable, will be randomized to either colectomy by laparoscopy or laparotomy. All patients that might be included will have a comprehensive geriatric assessment performed within the 30 days before randomization with the following scores: MMS (Mini Mental Score), ADL scale (Activities of Daily Living), IADL scale (Instrumental Activities of Daily Living), GDS (Geriatric Depression Scale) and TGUG test ("Timed Get-Up-and-Go" test).

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
75 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 75 years
  • Histologically proven colonic adenocarcinoma (> 15 cm from the anal margin) or precancerous colonic lesion non endoscopically resectable
  • Uncomplicated colonic tumor (no preoperative suspicion of invasion of adjacent structures as assessed by CT-scan (cT4), no tumoral perforation, or tumoral obstruction, or abscess, or hemorrhage)
  • No previous colonic cancer within the 5 last years
  • No peritoneal carcinosis on CT-scan
  • Patient able to fill in an auto-questionnaire alone or with some help
  • MMS (Mini Mental Score) ≥ 15
  • Given oral consent (formal informed consent is not required by French law for accepted procedures)

排除标准

  • Rectal cancer (≤ 15 cm from the anal margin)
  • Locally advanced (cT4) or complicated tumor requiring extended resection or emergency surgery
  • Synchronous colonic cancer
  • Scheduled need for synchronous intra-abdominal surgery, including surgery for liver metastases
  • Absolute contraindications to general anesthesia or prolonged pneumoperitoneum
  • Patient not able to tolerate colon surgery according to the global comprehensive geriatric assessment
  • Estimated life expectancy less than 6 months
  • Patient under guardianship
  • Other known active cancer (except nonmelanomatous skin cancer)
  • Patient not affiliated to the social security system
  • Previous colonic resection

研究组 & 干预措施

Laparotomy

Active Comparator

Open surgery

干预措施: Laparotomy (Procedure)

Laparoscopy

Experimental

Minimally invasive surgery

干预措施: Laparoscopy (Procedure)

结局指标

主要结局

Global postoperative morbidity in both arms

时间窗: At 30 days after the surgery

Postoperative morbidity is defined as any surgical or medical complications occurring up to 30 days after surgery. It will be collected using a standardized collection form during hospitalization and eventual subsequent consultations in case of patient discharge before then

次要结局

  • Postoperative mortality(Evaluated at 30 days and at 90 days after the surgery)
  • Number of examined lymph nodes(At surgery)
  • Type of resection (R0 or R1)(At surgery)
  • Pathological evaluation of mesocolic resection quality(At surgery)
  • Rate of readmission(Within the 30 days after discharge of the patient)
  • Health-related quality of life : Quality of Life Questionnaires (EORTC QLQ-C30)(At randomization and three months postoperatively)
  • Health-related quality of life : Quality of Life Questionnaires (EORTC QLQ-CR29)(At randomization and three months postoperatively)
  • Mini Mental State (MMS) Examination or Folstein test(Before randomization and three months postoperatively)
  • Katz Activities of Daily Living (ADL) scale(Before randomization and three months postoperatively)
  • Geriatric Depression Scale (GDS)(Before randomization and three months postoperatively)
  • Timed Get-up-and-go (TGUG)(Before randomization and three months postoperatively)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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