Can robotic tools make stomach cancer surgery safer and faster?
NCT ID NCT06881043
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
This study looks at whether robotic-assisted surgery using a vessel sealer can improve outcomes for people with locally advanced stomach cancer. The vessel sealer is a tool that cuts and seals blood vessels with less heat damage than older devices. Researchers will track 300 patients to see how many have complications within 30 days after surgery, how quickly they recover, and how well the cancer is controlled. The goal is to find out if this approach is safer and more effective than standard laparoscopic surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Robotic-assisted surgery using the Vessel Sealer Extend instrument
- What this could lead to
- If it works, this could establish robotic surgery with the vessel sealer as a safer, more precise option for advanced gastric cancer, reducing complications and speeding recovery.
- What could go wrong
- This is an observational study, not a randomized trial, so results may be influenced by patient selection. The benefits of robotic surgery for advanced gastric cancer remain debated, and complications are still possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2024
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with Primary gastric adenocarcinoma at the stage of cT2-4a, N-/+, M0.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age from over 18 to under 75 years * Primary gastric adenocarcinoma (papillary, tubular, mucinous, signet ring cell, or poorly differentiated) confirmed pathologically by endoscopic biopsy * cT2-4a, N-/+, M0 at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual 8th Edition * Preoperative abdominal enhanced CT and lung CT (or PET-CT) showed no distant metastasis * Performance status of 0 or 1 on ECOG (Eastern Cooperative Oncology Group) scale * ASA (American Society of Anesthesiology) class I to III * Written informed consent Exclusion Criteria: * Gastric multiple primary carcinoma or multiple primary cancer * History of previous upper abdominal surgery (except laparoscopic cholecystectomy) * History of previous gastric surgery (except ESD/EMR (Endoscopic Submucosal Dissection/Endoscopic Mucosal Resection ) for gastric cancer) * Preoperative gastric CT evaluation and chest and abdominal imaging evaluation were not performed before surgery, and the clinical stage of the tumor was not comprehensively evaluated * Enlarged or bulky regional lymph node (diameter over 3cm)supported by preoperative imaging * History of other malignant disease within the past 5 years * History of previous neoadjuvant chemotherapy or radiotherapy * History of unstable angina or myocardial infarction within the past 6 months * History of cerebrovascular accident within the past 6 months * History of continuous systematic administration of corticosteroids within 1 month * FEV1\<50% of the predicted values * Women during pregnancy or breast-feeding * Severe mental disorder * Emergency surgery due to complication (bleeding, obstruction or perforation) caused by gastric cancer * Preoperative evaluation requires combined organ resection * Requirement of simultaneous surgery for other disease
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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First Hospital of Jilin University
RECRUITINGChangchun, Jilin, 130012, China
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