Skip to main content
Clinical Trials/NCT06613399
NCT06613399
Not Yet Recruiting
N/A

A Randomized Controlled Study of Multi-technology Integration Total Mesorectal Excision (MTI-TME) Versus Conventional Total Mesorectal Excision (C-TME) for the Treatment of Middle and Distal Rectal Cancer.

The First Affiliated Hospital with Nanjing Medical University0 sites324 target enrollmentJanuary 1, 2025
ConditionsRectal Cancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Rectal Cancer
Sponsor
The First Affiliated Hospital with Nanjing Medical University
Enrollment
324
Primary Endpoint
anastomotic leakage rate
Status
Not Yet Recruiting
Last Updated
last year

Overview

Brief Summary

A multicenter, prospective, randomized, controlled clinical trial of multi-technology integration total mesorectal excision (MTI-TME) versus conventional total mesorectal excision (C-TME) for the treatment of middle and distal rectal cancer

Detailed Description

Currently, laparoscopic total mesorectal excision (TME) has become the standard procedure for treating middle and distal rectal cancer. Anastomotic leakage has always been one of the serious complications of TME surgery, and Anastomotic leakage not only increases the hospital expenses, but also brings physical discomfort and psychological pain to the patients. Furthermore, anastomotic leakage is associated with a heightened risk of anastomotic stenosis, compromised bowel function, delayed initiation of postoperative adjuvant therapy, increased local recurrence rates post-surgery, and diminished long-term survival outcomes. A report from the Netherlands indicates that anastomotic leakage serves as an independent prognostic factor for overall survival in patients diagnosed with rectal cancer. Prior studies have documented the incidence of anastomotic leakage to range between 3.6% and 21%, attributable to a confluence of various factors including technical complications, oncological considerations, and the patient\'s overall health status. Among these determinants, aspects such as blood supply adequacy, tension at the site of anastomosis, tissue quality, and anatomical positioning of the rectum are widely recognized as significant risk factors for developing anastomotic leaks.Currently, several strategies are employed to mitigate the incidence of anastomotic leakage, including preoperative proctocolectomy, anal decompression placement, vertical transverse resection of the rectum, and anastomotic reinforcement techniques. In our clinical practice, we have innovatively integrated multiple approaches: (1) preservation of the left colic artery (LCA); (2) high-level resection of the inferior mesenteric vein (IMV); (3) standardized mobilization of the splenic flexure along with left lateral colon; (4) multi-plane dissection of mesorectal flaps; and (5) selective reinforcement at the anastomosis. Our findings indicate that multi-technology integrated total mesorectal excision (MTI-TME) significantly reduces both preventive stoma rates and incidences of anastomotic leakage compared to conventional total mesorectal excision (C-TME), . However, there remains a lack of robust evidence-based medicine supporting MTI-TME\'s advantages in treating middle and distal rectal cancer; further research is urgently needed to provide additional clinical evidence.

Registry
clinicaltrials.gov
Start Date
January 1, 2025
End Date
December 31, 2027
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Participants must be aged 18 to
  • Histopathological examination of the preoperative biopsy confirms adenocarcinoma.
  • Preoperative MRI shows the tumor\'s lower margin is below the umbilical ligament.
  • High-resolution CT and MRI do not indicate suspicious distant metastasis.
  • Participants\' general condition is acceptable, with an ASA score of ≤3 before surgery.
  • Participants must sign an informed consent form.

Exclusion Criteria

  • Developing other malignant tumors within 5 years;
  • Multiple primary colorectal tumors;
  • Pregnant or lactating women;
  • Patients with severe mental disorders;
  • Severe intestinal diseases;
  • Poor general condition and uncontrolled comorbidities;
  • Ineligible for laparoscopic surgery;
  • Participating in other clinical trials.

Outcomes

Primary Outcomes

anastomotic leakage rate

Time Frame: 1 year

Secondary Outcomes

  • Operation time(During surgery)
  • intraoperative blood loss(During surgery)
  • 3-year overall suvival rate(3 years)
  • local recurrance rate(3 years)
  • 3-year disease-free survival rate(3 years)
  • 3-year mortality rate(3 years)
  • postoperative quality of life(3 years)
  • intestinal exhaust time(1 year)
  • postoperative pain(1 year)
  • colostomy rate(1 year)
  • hospital stay(1 year)
  • hospital cost(1 year)

Similar Trials