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Clinical Trials/NCT04527861
NCT04527861RecruitingNot Applicable

Oncologic Outcomes of Single-incision Laparoscopic Surgery Versus Conventional Laparoscopic Surgery for Colorectal Cancer: A Multi-center, Prospective, Open Label, Non-inferiority, Randomized Controlled Trial

Ruijin Hospital11 sites in 1 country710 target enrollmentStarted: April 8, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
710
Locations
11
Primary Endpoint
3-year disease free survival rate

Study Overview

Brief Summary

This study is designed to investigate long-term oncologic outcomes of single-incision laparoscopic surgery (SILS) compared to conventional laparoscopic surgery (CLS) for colorectal cancer.

Detailed Description

In order to improve cosmetic effect and reduce postoperative pain, single-incision laparoscopic surgery (SILS) is attracting increasing attention. SILS is considered to be the next major advance in the progress of minimally invasive surgical approaches to colorectal disease that is more feasible in generalized use. In most previous studies, SILS for colorectal cancer was feasible and short-term safe compared to conventional laparoscopic surgery (CLS) . However, there is still controversy over its potential better cosmetic effect and less postoperative pain. Moreover, the long-term oncologic outcomes are still inconclusive as only a few studies showed long-term survival data. Up to now, most studies were limited to their retrospective nature and small samples. So more studies, especially large-scale, randomized controlled trials are needed to establish the best indications for SILS for colorectal cancer.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 18 years < age ≤85 years
  • Tumor located in colon and high rectum ( the lower border of the tumor is above the peritoneal reflection)
  • Pathological or highly suspected colorectal carcinoma
  • Clinically diagnosed cT1-4aN0-2 M0 lesions according to the 8th Edition of AJCC Cancer Staging Manual
  • Tumor size of 5 cm or less
  • ECOG score is 0-1
  • ASA score is Ⅰ-Ⅲ
  • Informed consent

Exclusion Criteria

  • Body mass index (BMI) >35 kg/m2
  • The lower border of the tumor is located distal to the peritoneal reflection
  • Familial adenomatous polyposis (FAP)
  • Inflammatory bowel disease (IBD)
  • Multiple malignant colorectal tumors
  • Pregnant woman or lactating woman
  • Severe mental disease
  • Previous gastrointestinal surgery (except appendectomy )
  • Emergency operation due to complication (bleeding, perforation or obstruction) caused by colorectal cancer
  • Requirement of simultaneous surgery for other disease
  • Simultaneous or metachronous multiple cancers with disease-free survival ≤ 5 years

Arms & Interventions

Single-incision Laparoscopic Surgery

Experimental

Patients with colorectal cancer undergo single-incision laparoscopic surgery.

Intervention: Single-incision Laparoscopic Surgery (Procedure)

Conventional Laparoscopic Surgery

Active Comparator

Patients with colorectal cancer undergo conventional laparoscopic surgery(3~5 ports).

Intervention: Conventional Laparoscopic Surgery (Procedure)

Outcomes

Primary Outcomes

3-year disease free survival rate

Time Frame: 36 months after surgery

3-year disease free survival rate

Secondary Outcomes

  • Operative time(intraoperative)
  • Incision length(intraoperative)
  • Intraoperative blood loss(intraoperative)
  • Total incision length(intraoperative)
  • Conversion rate(intraoperative)
  • Early morbidity rate(30 days after surgery)
  • Lymph node detection(14 days after surgery)
  • Length of stay(1-14 days after surgery)
  • Tumor size(14 days after surgery)
  • Cosmetic effect(1 month, 6 months and 1 year after surgery)
  • The quality of life-Colorectal(1 month, 6 months and 1 year after surgery)
  • Postoperative recovery course(1-14 days after surgery)
  • Pain score(1-3 days after surgery)
  • Incisal margin(14 days after surgery)
  • The quality of life-Core(1 month, 6 months and 1 year after surgery)
  • 5-year overall survival rate(60 months after surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Zhao Ren

Chief Physicion

Ruijin Hospital

Study Sites (11)

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