跳至主要内容
临床试验/NCT06567756
NCT06567756尚未招募不适用

A Multicenter, Prospective, Randomized Controlled Clinical Trial of the Effect of Conformal Sphincter-preservation Operation Versus Intersphincteric Resection on Postoperative Anal Function in Patients With Low Rectal Cancer

Changhai Hospital0 个研究点目标入组 84 人开始时间: 2024年9月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
84
主要终点
Wexner incontinence score

研究概览

简要总结

In this clinical trial, the investigators compared anal function, genitourinary function, quality of life, perioperative safety, and oncological prognosis after CSPO for patients with low rectal cancer, using ISR as a control, to provide high-level evidence-based medical evidence for the choice of anorectal preservation surgical approaches for patients with low rectal cancer.

详细描述

The CSPO surgical approach is a series of targeted improvements designed primarily on the basis of analyzing the causes of poor postoperative function of the ISR, while building on research on the ultrastructure of the pelvic floor anal canal. For these reasons, the investigators designed the present study to compare anal function, quality of life, perioperative safety, and oncologic prognosis after CSPO for patients with low rectal cancer, using ISR surgery as a control, and to provide high-level evidence-based medical evidence for the choice of anorectal preservation surgical modalities for patients with low rectal cancer.

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

入选标准

  • Age: 18-75 years;
  • Pathologically confirmed: moderately & well-differentiated rectal cancer;
  • Low rectal cancer: lower edge of tumor ≦5cm from anal verge or ≦2cm from dentate line;
  • Tumor diameter: ≤3cm or <1/3 bowel circumference;
  • Tumor infiltration depth: cT1-2, Bordeaux/Rullier classification: type II-III;
  • Locally progressive rectal cancer (cT1-4N0-2M0): significant tumor downstaging and downgrading after preoperative neoadjuvant therapy, meeting the above criteria;
  • ASA score: I-III and ECOG score: 0-1;
  • Undergo elective TME for colorectal or colorectal-anal canal anastomosis;
  • Normal preoperative anal function: Wexner score <10, LARS score <20;
  • Agree to participate in the clinical trial and sign an informed consent form.

排除标准

  • Combination of synchronous or metachronous (within 5 years) malignant tumors;
  • Combined distant metastasis of the tumor;
  • Combined intestinal obstruction, intestinal perforation, or intestinal bleeding requiring emergency surgery;
  • Combined psychiatric disorders that do not allow them to understand and participate in the study;
  • Combined systemic diseases that cannot tolerate surgery;
  • Women who are pregnant or breastfeeding;
  • Other reasons, judged by the investigator, for not being suitable for participation in this clinical trial.

结局指标

主要结局

Wexner incontinence score

时间窗: 12 months after protective stoma closure

The scale was totaled from 0 to 20, with higher scores indicating more severe disease and poorer anal function.

次要结局

  • LARS scoreIncontinence Score(12 months after protective stoma closure)
  • Quality of Life Questionaire-Core 30(12 months after radical resection of rectal cancer and protective stoma closure)
  • Overall survival(3 years)
  • Clavien-Dindo complication grading(perioperative period)

研究者

申办方类型
Other
责任方
Sponsor

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