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A multicenter, prospective, randomized controlled clinical study on robotic and laparoscopic radical gastrectomy for locally advanced gastric cancer

A multicenter, prospective, randomized controlled clinical study on robotic and laparoscopic radical gastrectomy for locally advanced gastric cancer

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125346
Enrollment
Unknown
Registered
2026-05-26
Start date
2025-05-29
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Locally advanced gastric cancer

Interventions

Laparoscopic radical surgery for gastric cancer was performed:Laparoscopic completion of radical gastrectomy for gastric cancer
The method of radical surgery for gastric cancer by robot was adopted:The robot performed a radical gastrectomy for gastric cancer

Sponsors

The First Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age >18 years, <75 years; 2. The primary lesion in the stomach was diagnosed as gastric adenocarcinoma (papillary adenocarcinoma, tubular adenocarcinoma, mucinous adenocarcinoma, signet ring cell carcinoma, poorly differentiated adenocarcinoma, etc.) through endoscopic biopsy and histopathological examination; 3. Preoperative clinical stage was that of locally advanced gastric cancer (cT2-4a, N0-3, M0, according to the AJCC-8th TNM tumor staging); 4. Preoperative examination revealed no distant metastasis, and the tumor did not directly invade the pancreas, spleen or other adjacent organs; 5. Preoperative ECOG physical condition score: 0/1; 6. Preoperative ASA score: I - III; 7. Agree to participate in this study and sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Previous surgery for gastric malignancy, including submucosal resection and/or endomucosal resection; 2.Previous history of upper abdominal surgery (except laparoscopic cholecystectomy); 3.Preoperative imaging examinations indicated regional fusion and enlarged lymph nodes (maximum diameter =3cm); 4.Patients undergo emergency surgery due to bleeding or perforation of gastric tumors; 5.The patient has received definitive therapy before, such as radiotherapy, chemotherapy or immunotherapy; 6.The patient has a history of malignant tumors, or preoperative examination finds that it is combined with other malignant tumors; 7.ASA> Level 3; 8.Severe mental illness; 9.History of unstable angina or myocardial infarction within 6 months; 10.History of cerebral infarction or cerebral hemorrhage within 6 months; 11.Severe lung diseases with FEV1<50%; 12.Continuous systematic treatment with glucocorticoids within 1 month before the study; 13.Concurrent surgical treatment of other diseases is required; 14.Pregnant and lactating women;

Design outcomes

Primary

MeasureTime frame
Three-year disease-free survival rate;

Secondary

MeasureTime frame
Time of operation;Incidence of postoperative complications;The incidence of intraoperative complications;Operative actual;3-year overall survival rate;First time getting out of bed for activities, starting to pass gas, resuming solid food, resuming semi-solid food.;Number of lymph node dissections;

Countries

China

Contacts

Public ContactShi Yan

The First Affiliated Hospital of Army Medical University

shiyandoctor@sina.com+86 13752909448

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026