Transanal Versus Laparoscopic Total Mesorectal Excision for Rectal Cancer

Sponsor
Ruijin Hospital (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03413930
Collaborator
(none)
0
1
2
81
0

Study Details

Study Description

Brief Summary

This study is designed to evaluate the short-term and long-term results after transanal total mesorectal excision (TaTME) for the resection of mid and low rectal cancer compared with laparoscopic total mesorectal excision(LaTME).

Condition or Disease Intervention/Treatment Phase
  • Procedure: Transanal total mesorectal excision
  • Procedure: Laparoscopic total mesorectal excision
N/A

Detailed Description

Colorectal cancer (CRC) including rectal cancer is one of the most common gastrointestinal tumors, and its incidence is third in the world. At present,surgical treatments is the main means to cure CRC. Total mesorectal excision (TME) is the gold standard for rectal cancer surgery. Transanal total mesorectal excision (TaTME) was recently developed to overcome technical difficulties associated with LaTME and open TME. Most reports are retrospective studies. More studies, especially large-scale, randomized controlled trials are needed to establish the best indications for TaTME for mid and low rectal cancer.This is a single-center, open-label, non-inferiority, randomized controlled trial. A total of 120 eligible patients will be randomly assigned to TaTME group and LaTME group at a 1:1 ratio. It will provide valuable clinical evidence for the objective assessment of the oncological safety,efficacy and potential benefits of TaTME compared with LaTME for mid and low rectal cancer.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Single-center Prospective Randomized Controlled Study of the Transanal Total Mesorectal Excision Versus Laparoscopic Total Mesorectal Excision in Rectal Cancer
Anticipated Study Start Date :
Jun 1, 2019
Anticipated Primary Completion Date :
Mar 1, 2021
Anticipated Study Completion Date :
Mar 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: TaTME

Patients with mid or low rectal cancer undergo transanal total mesorectal excision.(assisted by laparoscopy to control the IMA)

Procedure: Transanal total mesorectal excision
Patients undergo transanal total mesorectal excision.(assisted by laparoscopy to control the IMA)

Active Comparator: LaTME

Patients with mid or low rectal cancer undergo laparoscopic total mesorectal excision.

Procedure: Laparoscopic total mesorectal excision
Patients undergo Laparoscopic total mesorectal excision.

Outcome Measures

Primary Outcome Measures

  1. Circumferential resection margin (CRM) [14 days after surgery]

    Positive rate of circumferential resection margin (pathological assessment)

Secondary Outcome Measures

  1. Completeness of mesorectum [14 days after surgery]

    Pathological assessment of completeness of the TME specimen(complete, near

  2. Lymph node detection [14 days after surgery]

    Lymph nodes harvested(numbers)

  3. Distal safety margin [14 days after surgery]

    Length of distal margin (millimeter,mm)

  4. Operative time [Intraoperative]

    Operative time(minutes)

  5. Intraoperative blood loss [Intraoperative]

    Estimated blood loss(milliliters,ml)

  6. Length of stay [1-30 days after surgery]

    Duration of hospital stay(days after surgery)

  7. Postoperative recovery course [1-14 days after surgery]

    Time to first ambulation, flatus, liquid diet and soft diet (hours after surgery)

  8. Early morbidity rate [30 days]

    Morbidity rate 30 days after surgery

  9. Pain score [1-3 days after surgery]

    Postoperative pain is recorded using the visual analog scale (VAS) pain score (0-10 points)tool on postoperative day 1, 2, 3 and the day of discharge

  10. 3-year disease free survival rate [36 months after surgery]

    3-year disease free survival rate

  11. 5-year overall survival rate [60 months after surgery]

    5-year overall survival rate

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18 years < age < 80 years

  • Body mass index (BMI) <30 kg/m2

  • Tumor located in mid and low rectum ( the lower border of the tumor is located distal to the peritoneal reflection)

  • Pathological rectal carcinoma

  • Clinically diagnosed cT1-3N0-2 M0 lesions according to the 7th Edition of AJCC Cancer Staging Manual with or without neoadjuvant therapeutic history

  • Tumor size of 5 cm or less

  • ECOG score is 0-1

  • ASA score is Ⅰ-Ⅲ

  • Informed consent

Exclusion Criteria:
  • Requiring a Mile's procedure

  • Fecal incontinence

  • History of inflammatory bowel disease

  • Pregnant woman or lactating woman

  • Severe mental disease

  • Intolerance of surgery for severe comorbidities

  • Previous abdominal surgery

  • Emergency operation due to complication (bleeding, perforation or obstruction) caused by rectal cancer

  • Requirement of simultaneous surgery for other disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ruijin Hospital North Shanghai Shanghai China 201821

Sponsors and Collaborators

  • Ruijin Hospital

Investigators

  • Study Chair: Yimei Jiang, MD, Ruijin Hospitla North

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Zhao Ren, Chief Physicion, Ruijin Hospital
ClinicalTrials.gov Identifier:
NCT03413930
Other Study ID Numbers:
  • RJ-TaTME-2018
First Posted:
Jan 29, 2018
Last Update Posted:
Feb 17, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Zhao Ren, Chief Physicion, Ruijin Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 17, 2020