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A prospective randomized controlled trial on reconstruction of mesentery with pedicled greater omentum flap for the prevention of anterior resection syndrome after total mesotomy for low rectal cancer

A prospective randomized controlled trial on reconstruction of mesentery with pedicled greater omentum flap for the prevention of anterior resection syndrome after total mesotomy for low rectal cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041887
Enrollment
Unknown
Registered
2021-01-09
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-03-30

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

Conditions

rectal cancer & low anterior rectal resection syndrome

Interventions

experimental group:TME + Dixon + greater omental pedicle flap transplantation
control group:TME + Dixon

Sponsors

Guangxi Medical University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Patients with rectal adenocarcinoma confirmed by colonoscopy pathological biopsy; 2.Age: 18-70 years; 3.Preoperative endoscopic ultrasonography staging and/or local imaging staging were T1-3NX, without distant metastasis (M0). 4.Complete TME is needed for low rectal cancer (= 18 kg/m2 and <= 34 kg/m2; 7.Signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Multiple primary or recurrent rectal cancer; 2.Combined abdominal and perineal resection (Mile's surgery); The reason of mental abnormality could not be assessed with the scale; 3.T1-stage rectal cancer patients meeting the criteria of transanal local resection; 4.Previous abdominal pelvic surgery or extensive abdominal adhesion; 5.Patients complicated with intestinal obstruction, intestinal perforation, intestinal bleeding and other situation requiring emergency surgery; 6.Patients with familial adenomatous polyposis, Lynch syndrome, and active inflammatory bowel disease; 7.Patients with anal fistula, perianal abscess, rectal prolapse, prolapse, anal stenosis, fecal incontinence and other anal organic or functional diseases; 8.Patients with severe liver and kidney function, cardiopulmonary function, coagulation dysfunction or combined with serious basic diseases cannot tolerate surgery; 9.Patients with consciousness disturbance or other cognitive dysfunction and a history of severe mental illness; 10.The presence of contraindications to MRI examination, such as cardiac pacemaker surgery, coronary intervention and coronary artery surgery bypass surgery; 11.Patients who are not eligible to participate in the study due to other clinical or laboratory conditions determined by the investigator.

Design outcomes

Primary

MeasureTime frame
LARS Score;Wexner Score;Anal pressure testing;Rectal defecography;

Countries

China

Contacts

Public ContactMo Xianwei

Guangxi Medical University Cancer Hospital

mo_xianwei@126.com+86 15677191500

Outcome results

None listed

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