Transvaginal NOSES Versus Conventional Laparoscopic Surgery for Right Hemicolectomy
Primary Purpose
Colon Cancer
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
NOSES VIIIA
laparoscopic surgery with mini-laparotomy
Sponsored by
About this trial
This is an interventional treatment trial for Colon Cancer
Eligibility Criteria
Inclusion Criteria:
- volunteer to participate and the informed consent signed;
- 18-75 years;
- female who have given birth;
- pathologically confirmed adenocarcinoma/high-grade intraepithelial neoplasia by preoperative colonoscopy and biopsy;
- preoperative CT or MRI indicates that the tumor diameter is no more than 5.0 cm;
- preoperative staging cT1-3NanyM0
- body mass index <30 kg/m2;
- willing to undergo laparoscopic right hemicolectomy
Exclusion Criteria:
- contraindications for laparoscopic surgery;
- emergency surgery due to acute intestinal obstruction, perforation or bleeding;
- distant metastasis;
- multiple colorectal cancer;
- has received preoperative chemoradiotherapy;
- with a history of other malignant tumors;
- unwilling to sign the informed consent or receive follow-up according to the study protocol.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
NOSES VIIIA
laparoscopic surgery with mini-laparotomy
Arm Description
totally laparoscopic right hemicolectomy with transvaginal natural orifice specimen extraction
laparoscopic right hemicolectomy with trans-abdominal extraction from a mini-laparotomy
Outcomes
Primary Outcome Measures
disease-free survival rate
disease-free survival rate
Secondary Outcome Measures
Full Information
NCT ID
NCT05495048
First Posted
August 9, 2022
Last Updated
August 9, 2022
Sponsor
Shanghai Minimally Invasive Surgery Center
1. Study Identification
Unique Protocol Identification Number
NCT05495048
Brief Title
Transvaginal NOSES Versus Conventional Laparoscopic Surgery for Right Hemicolectomy
Official Title
Transvaginal Natural Orifice Specimen Extraction Surgery Versus Conventional Laparoscopic Surgery With Mini-laparotomy in Right Hemicolectomy for Colon Cancer: a Randomised, Controlled, Phase 3, Non-inferiority Trial (NOSES VIIIA Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2023 (Anticipated)
Primary Completion Date
December 31, 2028 (Anticipated)
Study Completion Date
December 31, 2028 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Minimally Invasive Surgery Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
It is controversial that totally laparoscopic right hemicolectomy with transvaginal natural orifice specimen extraction (NOSES VIIIA) can provide non-inferior oncological outcomes compared to conventional laparoscopic surgery with mini-laparotomy in the treatment of right colon cancer. We aim to carry out a multicenter, open-lable, parallel, non-inferiority, phase III, randomized controlled clinical trial, which enrolls 356 female patients with cT1-3NxM0 right colon adenocarcinoma. They are randomly assigned to the experimental group (NOSES VIIIA) or the control group (laparoscopic surgery with mini-laparotomy) in a 1:1 ratio. Perioperative indicators, pathological results, quality of life and cosmetic evaluation will be compared between the two groups. Then, a three-year follow-up of these patients will provide evidence for long-term oncological outcomes of NOSES VIIIA.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
356 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
NOSES VIIIA
Arm Type
Experimental
Arm Description
totally laparoscopic right hemicolectomy with transvaginal natural orifice specimen extraction
Arm Title
laparoscopic surgery with mini-laparotomy
Arm Type
Active Comparator
Arm Description
laparoscopic right hemicolectomy with trans-abdominal extraction from a mini-laparotomy
Intervention Type
Procedure
Intervention Name(s)
NOSES VIIIA
Intervention Description
totally laparoscopic right hemicolectomy with transvaginal natural orifice specimen extraction
Intervention Type
Procedure
Intervention Name(s)
laparoscopic surgery with mini-laparotomy
Intervention Description
laparoscopic right hemicolectomy with trans-abdominal extraction from a mini-laparotomy
Primary Outcome Measure Information:
Title
disease-free survival rate
Description
disease-free survival rate
Time Frame
3 years after surgery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
volunteer to participate and the informed consent signed;
18-75 years;
female who have given birth;
pathologically confirmed adenocarcinoma/high-grade intraepithelial neoplasia by preoperative colonoscopy and biopsy;
preoperative CT or MRI indicates that the tumor diameter is no more than 5.0 cm;
preoperative staging cT1-3NanyM0
body mass index <30 kg/m2;
willing to undergo laparoscopic right hemicolectomy
Exclusion Criteria:
contraindications for laparoscopic surgery;
emergency surgery due to acute intestinal obstruction, perforation or bleeding;
distant metastasis;
multiple colorectal cancer;
has received preoperative chemoradiotherapy;
with a history of other malignant tumors;
unwilling to sign the informed consent or receive follow-up according to the study protocol.
12. IPD Sharing Statement
Learn more about this trial
Transvaginal NOSES Versus Conventional Laparoscopic Surgery for Right Hemicolectomy
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