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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
Shanghai Minimally Invasive Surgery Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colon Cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

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

    First Posted
    August 9, 2022
    Last Updated
    August 9, 2022
    Sponsor
    Shanghai Minimally Invasive Surgery Center
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    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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