Assessment of Robotic Versus Laparoscopic Gastrectomy for GC Patients With Intraoperative Technical Complexity
1 other identifier
observational
3,534
1 country
1
Brief Summary
While robotic gastrectomy (RG) is increasingly used in gastric cancer surgery, its potential advantages over laparoscopic gastrectomy (LG) in Intraoperative technical complexity (ITC) cases remain debated.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2016
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2024
CompletedFirst Submitted
Initial submission to the registry
December 22, 2024
CompletedFirst Posted
Study publicly available on registry
December 30, 2024
CompletedJune 11, 2025
June 1, 2025
2.8 years
December 22, 2024
June 6, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Overall survival
Telephone follow-up
Within 3 years after surgery
Secondary Outcomes (2)
recurrence
36 months
Postoperative complications
30 days after surgery
Study Arms (2)
RG group
Patients undergoing robotic gastrectomy
LG group
Patients undergoing laparoscopic gastrectomy
Eligibility Criteria
Patients with pathologically confirmed T1-4aN0-3bM0 gastric adenocarcinoma who underwent radical RG or LG between August 2016 and June 2019 at eight high-volume tertiary teaching hospitals in China
You may qualify if:
- Patients with postoperatively histologically confirmed T1-4aN0-3bM0 gastric adenocarcinoma who underwent RG or LG
You may not qualify if:
- Remnant gastric cancer
- Previous malignant
- ASA class \>3
- Use of indocyanine green
- Neoadjuvant chemotherapy
- Loss to follow-up
- Combined resection
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Fujian Medical University Union Hospital
Fuzhou, Fujian, 350001, China
Study Officials
- PRINCIPAL INVESTIGATOR
Chang-Ming Huang, PhD
Fujian Medical University Union Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
December 22, 2024
First Posted
December 30, 2024
Study Start
August 1, 2016
Primary Completion
June 1, 2019
Study Completion
July 1, 2024
Last Updated
June 11, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share