Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT04037956

Tubeless NOSES Versus Laparoscopic Radical Resection for Rectosigmoid Cancers

Led by Sixth Affiliated Hospital, Sun Yat-sen University · Updated on 2022-03-31

458

Participants Needed

1

Research Sites

426 weeks

Total Duration

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AI-Summary

What this Trial Is About

This study is designed to evaluate the short-term and long-term results after Tubeless NOSES for the resection of Rectosigmoid Cancers compared with traditional laparoscopic radical resection.

CONDITIONS

Official Title

Tubeless NOSES Versus Laparoscopic Radical Resection for Rectosigmoid Cancers

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically or cytologically confirmed rectosigmoid cancers
  • Clinical stage T1-3 N0-2 M0
  • Tumors located on peritoneal reflection with size no more than 3 cm
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2
  • American Society of Anesthesiologists (ASA) physical status score of I to III
  • Body mass index (BMI) of 30 kg/m2 or less
  • Willing and able to comply with scheduled visits, treatment plans, and laboratory testing
Not Eligible

You will not qualify if you...

  • Heart, lung, liver, kidney, or other organ function problems that make surgery unsafe
  • History of treated colorectal cancer
  • Medical conditions like intestinal obstruction, perforation, bleeding requiring emergency surgery
  • Previous malignancies
  • History of inflammatory bowel disease (IBD) or familial adenomatous polyposis (FAP)
  • Participation in another clinical trial within 28 days before randomization
  • History of severe mental illness
  • Pregnant or breastfeeding women
  • Considered unsuitable for participation by the researchers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Sixth Affiliate Hospital of Sun Yat-Sen University

Guangzhou, Guangdong, China

Actively Recruiting

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Research Team

Y

Yanxin Luo, MD,PHD

CONTACT

J

Jinxin Lin, MD,PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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