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3D Versus 2D Laparoscopic Total Gastrectomy With Splenic Hilum Lymph Nodes Dissection

3D Versus 2D Laparoscopic Total Gastrectomy With Spleen-preserving Splenic Hilum Lymph Nodes Dissection for Advanced Proximal Gastric Cancer: A Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02984787
Enrollment
480
Registered
2016-12-07
Start date
2017-01-31
Completion date
2020-01-31
Last updated
2016-12-07

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

Conditions

Splenic Hilum Lymph Nodes Dissection

Keywords

Gastric Cancer, 3D, 2D

Brief summary

The investigators will perform a prospective randomized comparison between 3D and 2D laparoscopic total gastrectomy with splenic hilum lymph nodes dissection.

Detailed description

A prospective randomized comparison of 3D and 2D laparoscopic surgery for advanced gastric cancer with spleen-preserving splenic hilum lymph nodes dissection will be performed, to evaluate the safety and feasibility for the extensive application of the novel 3D laparoscopic technique. The evaluation parameters are number of group No.10 lymph nodes harvested, perioperative clinical efficacy, postoperative life quality and 3-year survival and recurrence rates.

Interventions

PROCEDURE3D Laparoscopic total gastrectomy

When participants with advanced proximal gastric cancer are randomized in the 3D laparoscopic-assisted totalgastrectomy (3D-LTG) group, they will received 3D-LTG with spleen-preserving splenic hilum lymph nodes dissection

PROCEDURE2D Laparoscopic total gastrectomy

When participants with advanced proximal gastric cancer are randomized in the 2D laparoscopic-assisted totalgastrectomy (2D-LTG) group, they will received 2D-LTG with spleen-preserving splenic hilum lymph nodes dissection

Sponsors

Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Primary proximal gastric adenocarcinoma confirmed pathologically by endoscopic biopsy; 2. cT2-4aN0-3M0 at preoperative evaluation according to AJCC Cancer Staging Manual, 7th Edition. 3. Eastern Cooperative Oncology Group (ECOG): 0 or 1; 4. American Society of Anesthesiologists (ASA) score: Ⅰto Ⅲ; 5. Written informed consent.

Exclusion criteria

1. Pregnant or breast-feeding women; 2. Severe mental disorder; 3. Previous upper abdominal surgery (except laparoscopic cholecystectomy); 4. Previous gastrectomy, endoscopic mucosal resection, or endoscopic submucosal dissection; 5. Enlarged or bulky regional lymph node diameter larger than 3 cm based on preoperative imaging; 6. Other malignant disease within the past 5 years; 7. Previous neoadjuvant chemotherapy or radiotherapy; 8. Contraindication to general anesthesia (severe cardiac and/or pulmonary disease); 9. Emergency surgery due to a complication (bleeding, obstruction, or perforation) caused by gastric cancer.

Design outcomes

Primary

MeasureTime frame
Number of splenic hilum lymph nodes harvested7 days

Secondary

MeasureTime frameDescription
Operative timeIntraoperativeIt will be assessed with the unit of minute.
Operative blood lossIntraoperativeIt will be assessed with the unit of ml.
Time of splenic hilum lymph nodes dissectionIntraoperativeIt will be assessed with the unit of minute
Number of total lymph nodes harvested7 days
Early complication rate30 daysThe early complication rate is defined as the event observed during operation and within 30 days after surgery.
Quality of life1 yearIt will be assessed with questionnaire of WHO-QOL-100 (WHO was short for world health organization)
3-year disease free survival rate3 years
3-year overall survival rate3 years
Poster-operative recovery course30 daysTime to first ambulation (unit of hour), flatus (unit of hour), liquid diet (unit of hour) and duration of hospital stay (unit of day) are used to assess the postoperative recovery course.

Countries

China

Contacts

Primary ContactHongqing Xi, Master
chenlinbj@sina.com86-13801290395

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026