Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05970133

Robotic Versus Laparoscopy NOSE for Stage I-III Left-sided Colon Cancer

Led by National Taiwan University Hospital · Updated on 2024-09-20

300

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this project, the investigator aims to provide the level 1 evidence for the comparison of robotic versus laparoscopic NOSE for the surgery of stage I-III colorectal cancer. the investigator hypothesize that, with the increased maneuverability of the current robotic system, robotic surgery will be a good option for patients with stage I-III colorectal cancer requiring a NOSE procedure.

CONDITIONS

Official Title

Robotic Versus Laparoscopy NOSE for Stage I-III Left-sided Colon Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Primary colon cancers located at the left sided colonic anatomic location, including distal transverse colon, colonic splenic flexure, descending colon, sigmoid descending colonic junction, sigmoid colon and upper rectum that required the mobilization of colonic splenic flexure to facilitate a curative resection and transanal specimen extraction
  • TNM Stage I-III adenocarcinomas
  • Curative and elective surgery
  • American Society of Anesthesiology (ASA) class I to III patients
  • Age over 18 years
Not Eligible

You will not qualify if you...

  • Cecal, ascending, the proximal and middle transverse colon cancers; and the middle or lower rectal cancers
  • Emergency or palliative surgery
  • Evidence of disseminated disease or adjacent organ invasion
  • Primary tumor mass larger than 8 cm in diameter
  • Morbidly obese patients, that is, body mass index (BMI) 40 kg/m2 or higher
  • Previous major surgery of upper abdomen or pelvis

AI-Screening

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Trial Site Locations

Total: 1 location

1

National Taiwan University Hospital

Taipei, Taiwan, 100

Actively Recruiting

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Research Team

J

Jin-Tung LIANG, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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