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Laparoscopic-endoscopic combined surgery for early gastric cancer

Laparoscopic-endoscopic combined surgery for early gastric cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124729
Enrollment
Unknown
Registered
2026-05-15
Start date
2026-05-16
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Early gastric cancer

Interventions

Early-stage gastric cancer observation group:None

Sponsors

Affiliated Hospital of Jiangsu University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 65 years old; 2. Preoperative diagnosis of early gastric cancer confirmed by gastroscopy biopsy pathology; 3. Through MDT collaboration assessment: The pathology department determined the tumor differentiation through immunohistochemistry, the endoscopy department determined the tumor stage and invasion depth through endoscopic ultrasound, and the gastro surgery department, digestive internal medicine department, and anesthesia department jointly evaluated whether it met the indications of LECS + ICG-SNNS; 4. No anti-tumor treatment such as chemotherapy or radiotherapy was received before the surgery; 5. The patient and his/her family gave informed consent and signed the consent form; 6. There were no contraindications for surgery, anesthesia, or ICG use, and the physical condition was tolerable for the surgery; 7. The patient and his/her family could cooperate to complete the 12-month postoperative follow-up and related re-examination items.

Exclusion criteria

Exclusion criteria: 1. Those who do not meet the indications of LECS+ICG-SNNS after MDT collaborative assessment; 2. Age less than 18 years or more than 65 years; 3. Complicated with severe underlying diseases: cardiac function > grade II (NYHA), severe hypertension (systolic blood pressure >= 180 mmHg or diastolic blood pressure >= 110 mmHg), severe liver and kidney dysfunction (Child-Pugh >= 10 points, creatinine clearance rate < 25 ml/min), respiratory insufficiency, coagulation dysfunction; 4. Allergic to indocyanine green (ICG), anesthetics, cephalosporin antibiotics and other commonly used perioperative drugs; 5. Complicated with complete gastrointestinal obstruction, emergency surgery or palliative surgery; 6. Surgery requires combined resection of other organs such as spleen and pancreas; 7. Malnutrition or severe malnutrition (albumin <= 0 g/L, BMI < 18); 8. Pregnant, lactating women or those with pregnancy plans within 1 month after the trial (including male participants); 9. Those who have participated in other clinical trials in the past 3 months; 10. The sponsors, investigators or their family members directly involved in the trial; 11. Pathologically confirmed as advanced gastric cancer or other types of tumors (squamous cell carcinoma, neuroendocrine tumor, gastrointestinal stromal tumor, etc.).

Design outcomes

Primary

MeasureTime frame
MDT assessment consistency rate;Tumor resection rate;Detection rate of sentinel lymph nodes;

Secondary

MeasureTime frame
First bowel movement time;PG-SGA Nutritional Score;

Countries

China

Contacts

Public ContactXin Fan

Affiliated Hospital of Jiangsu University

drfanxin@163.com+86 511 8508 2208

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026