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临床试验/NCT04016948
NCT04016948Unknown不适用

A Multicenter Randomized Study of Real-time In-vivo Confocal Laser Endomicroscopy Optical Biopsy for Distal Margin in Low Rectal Cancer Compared to Intraoperative Frozen Section

Nanfang Hospital, Southern Medical University1 个研究点 分布在 1 个国家目标入组 146 人开始时间: 2017年6月28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
146
试验地点
1
主要终点
Accuracy of optical biopsy

研究概览

简要总结

This is a multi-center prospective randomized controlled study. In this study, the investigators will use confocal laser endomicroscopy to make real-time in vivo optical biopsy of distal margin in rectal cancer surgery and help surgeons to make surgical decision.The investigators also assess the accuracy of CLE optical biopsy, compared with intra-operative frozen section.

详细描述

In low rectal cancer surgery, how to select the precise dissection plane and optimal surgical procedure is an important challenge for surgeons. In current clinic, surgeons select dissection plane by a comprehensive judgment of pre-operative pelvis MRI, colonoscopy and digital rectal examination, then through submitting the "doughnut" after cutting and anastomosis to intra-operative frozen section (IFS) to definite whether there is residual tumor in distal margin (DM). However, IFS can only make diagnosis using the tissue specimen in vitro and time-consuming. Once the IFS confirm positive margin, it always means anal resection should be implemented to ensure radical treatment. Therefore, if there is a real-time in situ examination method to evaluate DM in vivo, it will bring great benefits to both surgeons and patients.

Confocal laser endomicroscopy (CLE) had been widely used in medical field to diagnose colorectal disease, but it is seldom applied in surgical filed especially in rectal cancer to make optical biopsy and help surgical decision-making. Therefore, the investigators hypothesize that CLE can real-time in situ evaluate DM during surgery in rectal cancer and its accuracy is non-inferior to intra-operative frozen section.

In this study, the investigators will randomly assign patients to the experimental group (CLE optical biopsy) and control group (IFS). Using H-E staining pathological diagnosis as golden standard, the accuracy, sensitivity and specificity of both CLE optical biopsy and IFS will be evaluated and compared. And the investigators will also evaluate patients' postoperative urinary function, defection function and quality of life through a year follow-up.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Ages from 18 to 70 years.
  • •Rectal tumor confirmed pathologically by endoscopic biopsy.
  • •The distance from lower edge of tumor to the dentate line is less than 5cm.
  • •Plan to perform curative resection.
  • •ASA(American Society of Anesthesiology)score class I,II,or III.
  • •Able to provide written informed consent.

排除标准

  • •Intestinal perforation or acute intestinal obstruction.
  • •Multiple distant metastasis and can not R0 resection.
  • •T4b according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual Seventh Edition.
  • •Pregnancy or breastfeeding.
  • •Impaired renal function
  • •American Society of Anesthesiology score (ASA) class IV or V.
  • •Unable or refuse to provide written informed consent.

研究组 & 干预措施

Probe-based confocal laser endomicroscopy(pCLE)

Experimental

Confocal laser endomicroscopy optical biopsy will be performed in surgery for patients assigned to this group

干预措施: Probe-based confocal laser endomicroscopy optical biopsy (Device)

Intra-operative frozen section(IFS)

Active Comparator

Intra-operative frozen section will be performed for patients assigned to this group

干预措施: Intra-operative frozen section (Device)

结局指标

主要结局

Accuracy of optical biopsy

时间窗: One week after surgery

Accuracy of confocal laser endomicroscopy optical biopsy of distal margin is determined by the pathology result.

次要结局

  • Sensitivity and Specificity(One week after surgery)
  • Operation related indexes(One week after surgery)
  • Postoperative function recovery(Up to 12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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