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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03426514
Other study ID # RJ-TLSC-2018
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 25, 2018
Est. completion date March 2025

Study information

Verified date February 2020
Source Ruijin Hospital
Contact Ren Zhao, MD
Phone +86-18917762018
Email rjzhaoren@139.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is designed to evaluate the short-term and long-term results after three-port laparoscopic surgery for colorectal cancer(TLSC) compared with conventional laparoscopic surgery for colorectal cancer(CLSC).


Description:

At present,surgical treatments is the main means to cure colorectal cancer(CRC).The use of four or more ports has been routine in most laparoscopic colorectal resections. However,the drawbacks are the need for added manpower, consisting of another assistant to provide counter-traction, as well as costs and the unaesthetic effects of additional ports. In order to minimize surgical trauma, improve cosmesis ,reduce manpower,single-incision laparoscopic surgery (SILS) is attracting increasing attention. But it is challenging and highly demanding techniques. Becoming proficient at three-port laparoscopic surgery can make the transition to SILS more nature.Few studies about three-port laparoscopic surgery for colorectal cancer(TLSC) have been reported currently.More studies, especially large-scale, randomized controlled trials are needed to establish the best indications for TLSC. This is a single-center, open-label, non-inferiority, randomized controlled trial. A total of 282 eligible patients will be randomly assigned to TLSC group and CLSC group at a 1:1 ratio. It will provide valuable clinical evidence for the objective assessment of the the feasibility, safety, and potential benefits of TLSC compared with CLSC.


Recruitment information / eligibility

Status Recruiting
Enrollment 282
Est. completion date March 2025
Est. primary completion date March 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Body mass index (BMI) <30 kg/m2

- Tumor located in colon and high rectum (the lower border of the tumor is above the peritoneal reflection)

- Pathological colorectal carcinoma

- Clinically diagnosed cT1-4aN0-2 M0 lesions according to the 7th Edition of AJCC Cancer Staging Manual with or without neoadjuvant therapeutic history

- ECOG score is 0-1

- ASA score is ?-?

- Informed consent

Exclusion Criteria:

- Previous gastrointestinal surgery

- History of inflammatory bowel disease

- History of familial adenomatous polyposis(FAP)

- Pregnant woman or lactating woman

- Severe mental disease

- Intolerance of surgery for severe comorbidities

- Emergency operation due to complication (bleeding, perforation or obstruction) caused by colorectal cancer

- Requirement of simultaneous surgery for other disease

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Three-port Laparoscopic Surgery
Patients undergo three-port laparoscopic surgery. The surgery will be completed by a surgeon and a camera-person without another assistant. The surgeon will adjust surgical position to expose the operative field with the help of gravity. All the orther operative procedures are the same as conventional laparoscopic surgery.
Conventional Laparoscopic Surgery
Patients undergo conventional laparoscopic surgery(4 or more ports).The surgery will be routinely completed by a surgeon,a camera-person and another assistant to provide counter-traction.

Locations

Country Name City State
China Ruijin Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Ruijin Hospital

Country where clinical trial is conducted

China, 

References & Publications (2)

Seow-En I, Tan KY, Mohd Daud MA, Seow-Choen F. Traditional laparoscopic colorectal resections can be performed effectively using a three-port technique. Tech Coloproctol. 2011 Mar;15(1):91-3. doi: 10.1007/s10151-010-0660-6. Epub 2011 Jan 14. — View Citation

Tawfik Amin A, Elsaba TM, Amira G. Three ports laparoscopic resection for colorectal cancer: a step on refining of reduced port surgery. ISRN Surg. 2014 Mar 12;2014:781549. doi: 10.1155/2014/781549. eCollection 2014. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Early morbidity rate morbidity rate 30 days after surgery 30 days after surgery
Secondary Operative time Operative time(minutes) intraoperative
Secondary Intraoperative blood loss Estimated blood loss(milliliters,ml) intraoperative
Secondary Lymph node detection Lymph nodes harvested(numbers) 14 days after surgery
Secondary Proximal resection margin Length of proximal margin (centimeters,cm) 14 days after surgery
Secondary Distal resection margin Length of distal margin (centimeters,cm) 14 days after surgery
Secondary Length of stay Duration of hospital stay(days after surgery) 1-14 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 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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