Rectal Cancer Clinical Trial
Official title:
Single-center Prospective Randomized Controlled Study of the Transanal Total Mesorectal Excision Versus Laparoscopic Total Mesorectal Excision in Rectal Cancer
NCT number | NCT03413930 |
Other study ID # | RJ-TaTME-2018 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2019 |
Est. completion date | March 2026 |
Verified date | February 2020 |
Source | Ruijin Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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).
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | March 2026 |
Est. primary completion date | March 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
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 ?-? - 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 |
Country | Name | City | State |
---|---|---|---|
China | Ruijin Hospital North | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Ruijin Hospital |
China,
Deijen CL, Velthuis S, Tsai A, Mavroveli S, de Lange-de Klerk ES, Sietses C, Tuynman JB, Lacy AM, Hanna GB, Bonjer HJ. COLOR III: a multicentre randomised clinical trial comparing transanal TME versus laparoscopic TME for mid and low rectal cancer. Surg Endosc. 2016 Aug;30(8):3210-5. doi: 10.1007/s00464-015-4615-x. Epub 2015 Nov 4. — View Citation
Fernández-Hevia M, Delgado S, Castells A, Tasende M, Momblan D, Díaz del Gobbo G, DeLacy B, Balust J, Lacy AM. Transanal total mesorectal excision in rectal cancer: short-term outcomes in comparison with laparoscopic surgery. Ann Surg. 2015 Feb;261(2):221-7. doi: 10.1097/SLA.0000000000000865. — View Citation
Simillis C, Hompes R, Penna M, Rasheed S, Tekkis PP. A systematic review of transanal total mesorectal excision: is this the future of rectal cancer surgery? Colorectal Dis. 2016 Jan;18(1):19-36. doi: 10.1111/codi.13151. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Circumferential resection margin (CRM) | Positive rate of circumferential resection margin (pathological assessment) | 14 days after surgery | |
Secondary | Completeness of mesorectum | Pathological assessment of completeness of the TME specimen(complete, near | 14 days after surgery | |
Secondary | Lymph node detection | Lymph nodes harvested(numbers) | 14 days after surgery | |
Secondary | Distal safety margin | Length of distal margin (millimeter,mm) | 14 days after surgery | |
Secondary | Operative time | Operative time(minutes) | Intraoperative | |
Secondary | Intraoperative blood loss | Estimated blood loss(milliliters,ml) | Intraoperative | |
Secondary | Length of stay | Duration of hospital stay(days after surgery) | 1-30 days after surgery | |
Secondary | Postoperative recovery course | Time to first ambulation, flatus, liquid diet and soft diet (hours after surgery) | 1-14 days after surgery | |
Secondary | Early morbidity rate | Morbidity rate 30 days after surgery | 30 days | |
Secondary | Pain score | 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 | 1-3 days after surgery | |
Secondary | 3-year disease free survival rate | 3-year disease free survival rate | 36 months after surgery | |
Secondary | 5-year overall survival rate | 5-year overall survival rate | 60 months after surgery |
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