About this trial
This is a retrospective, multicenter cohort study to compare short- and long-term outcomes between robotic and laparoscopic hemicolectomy of right colon cancer.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
1.Underwent radical right hemicolectomy by Da Vinci robotic or laparoscopic surgery 2.Postoperative pathology confirmed right colon adenocarcinoma (pT2-T4aNxM0; including cecal adenocarcinoma, ascending colon adenocarcinoma, hepatic flexure colon adenocarcinoma, and proximal transverse colon adenocarcinoma) 3.Complete clinical data and pathological results available
Disqualifiers
1.Received neoadjuvant therapy prior to surgery 2.History of other malignancies in the past 5 years (except cured cervical carcinoma in situ, basal cell carcinoma, or squamous cell carcinoma of the skin) 3.Distant metastases (e.g., liver, lung) or extensive abdominal/pelvic metastases confirmed by contrast-enhanced CT, PET-CT, or intraoperative exploration 4.Comorbid neurological/psychiatric disorders impairing ability to express informed consent 5.Poor systemic condition with contraindications to general anesthesia 6.Severe obesity (BMI >35 kg/m²) 7.Severe widespread abdominal adhesions precluding safe pneumoperitoneum establishment 8.Emergency surgery due to tumor perforation or obstruction 9.Refusal to provide informed consent
Trial population
The procedures were performed by 16 surgeons from 16 participating centers. Both primary surgeons and assistants completed standardized training in robotic and laparoscopic surgical techniques and obtained certification. Each center performs over 100 robotic- or laparoscopic-assisted radical right hemicolectomies annually. Primary surgeons had performed at least 50 cases of both robotic and laparoscopic-assisted radical right hemicolectomy.
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
3-year overall survival (OS) rate and 3-year disease-free survival (DFS) rate
Secondary outcomes
Operative time
Intraoperative blood loss
Time to first flatus/bowel movement
Time to liquid diet initiation
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
The First Affiliated Hospital of Nanchang University
Lead sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Collaborator
Fudan University
Collaborator
The Second Affiliated Hospital of Harbin Medical University
Collaborator
Three Gorges Hospital of Chongqing University
Collaborator
The Affiliated Hospital of Qingdao University
Collaborator
The First Affiliated Hospital of Zhengzhou University
Collaborator
Tianjin Third Central Hospital
Collaborator
Shandong University Second Hospital
Collaborator
Nanfang Hospital, Southern Medical University
Collaborator
Huadong Hospital
Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University
Collaborator
Second Xiangya Hospital of Central South University
Collaborator
Jiangxi Provincial People's Hopital
Collaborator
Pingxiang People 's Hospital
Collaborator
Ganzhou City People's Hospital
Collaborator
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