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Effect of transanal total mesenteric resection versus laparoscopic total mesorectal excision in the clinic effect and postoperative anal function in patients with low rectal caner: a single-center, prospective, randomized controlled study

Effect of transanal total mesenteric resection versus laparoscopic total mesorectal excision in the clinic effect and postoperative anal function in patients with low rectal caner: a single-center, prospective, randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052459
Enrollment
Unknown
Registered
2021-10-26
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rectal cancer

Interventions

experimental group:Transanorectal total mesorectal excision

Sponsors

The First Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Subjects aged 18-75 years; 2. Biopsy pathology confirmed rectal adenocarcinoma; 3. MRI and/or rectosigmoid endoscopy showed that the distance between the lower edge of the tumor and the anal verge was less than or equal to 5cm; 4. High-resolution MRI judges rectal cancer as T2-T3b, N0; 5. No distant metastasis of tumor in preoperative examination; 6. ECOG (Eastern Cooperative Oncology Group) determines the clinical condition as grade 0-2; 7. Subjects signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Radiotherapy and chemotherapy for rectal cancer before enrollment; 2. History of other tumors, non-adenocarcinoma rectal malignant tumor or rectal malignant tumor occurring on the basis of inflammatory bowel disease; 3. Emergency surgery is required due to intestinal obstruction, perforation, bleeding, etc.; 4. Pregnant and lactating women; 5. The investigator judges that the compliance is poor or not suitable for this clinical trial.

Design outcomes

Primary

MeasureTime frame
Local Recurrence;Overall survival;disease free survival;anal function;

Secondary

MeasureTime frame
R0 resection rate;Quality of surgical specimen;Surgical complications within 30 days;

Countries

China

Contacts

Public ContactZheng Jianyong

The First Affiliated Hospital of Air Force Medical University

zhjy68@163.com+86 13891385899

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026