Skip to main content
Clinical Trials/NCT03708783
NCT03708783
Unknown
Not Applicable

Study on Short and Long-term Outcome of Laparoscopic Spleen-Preserving No. 10 Lymph Node Dissection for Advanced Middle or Upper Third Gastric Cancer

Peking University Cancer Hospital & Institute1 site in 1 country170 target enrollmentJuly 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gastric Cancer
Sponsor
Peking University Cancer Hospital & Institute
Enrollment
170
Locations
1
Primary Endpoint
the incidence of postoperative complications within 30 days
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to explore the safety and feasibility of laparoscopic spleen-preserving No. 10 lymph node dissection for patients with advanced middle or upper third gastric cancer.

Detailed Description

Radical resection is the primary treatment for patients with advanced middle or upper third gastric cancer. And D2 lymphadenectomy, including No. 10 lymph node dissection, should be performed according to the Japanese treatment guidelines for gastric cancer. Because of the complexity of the anatomy around the spleen, spleen-preserving No. 10 lymph node dissection is difficult. Although Professor Huang from Fujian Medical University Union Hospital has proposed the "Huang's three-step maneuver" to dissect No. 10 lymph node with preserved spleen laparoscopically, such method is far from popularized, especially in North China. In addition, the safety, feasibility and oncological efficacy of this method was not confirmed in such area, either. In this study, a prospective, single center, single-arm, non-inferiority clinical trial will be conducted to evaluate the short and long-term outcome of the laparoscopic spleen-preserving No. 10 lymph node dissection for patients with locally advanced middle or upper third gastric cancer in Beijing.

Registry
clinicaltrials.gov
Start Date
July 1, 2018
End Date
December 30, 2023
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Peking University Cancer Hospital & Institute
Responsible Party
Principal Investigator
Principal Investigator

Xiangqian Su

Chief of GI surgery IV

Peking University Cancer Hospital & Institute

Eligibility Criteria

Inclusion Criteria

  • Patients age older than 18 years (including 18 years old);
  • The primary lesion is located in the upper or middle third of the stomach, including Siewert II type and Siewert III type adenocarcinoma of the esophagogastric junction;
  • Pathologically confirmed primary gastric adenocarcinoma by endoscopic biopsy (including papillary, tubular, mucinous, signet ring cell and poorly differentiated adenocarcinoma);
  • Preoperative cancer stage cT2-4aN0-3M0 (according to AJCC-7th TNM staging);
  • The Eastern Cooperative Oncology Group performance status of 0 or 1;
  • The American Society of Anesthesiology classes of I, II or III;
  • Signed Informed consent.

Exclusion Criteria

  • Pregnant or lactating women;
  • Suffering from severe mental disorder;
  • Previous gastrectomy, including endoscopic submucosal dissection and endoscopic mucosal resection;
  • Integrated or enlarged lymph node with maximum diameter larger than 3 cm according to preoperative imaging, including significantly enlarged or bulky No. 10 lymph nodes;
  • Siewert I type adenocarcinoma of the esophagogastric junction;
  • Other malignant diseases (within 5 years);
  • Other illnesses needed operation concurrently;
  • Complications (bleeding, perforation or obstruction) required emergency surgery due to primary gastric malignancy;
  • Pulmonary function tests FEV1 less than 50% of predicted value;
  • Patient suffered from bleeding tendency disease such as hemophilia or took anti-coagulant medication due to deep vein thrombosis.

Outcomes

Primary Outcomes

the incidence of postoperative complications within 30 days

Time Frame: 30 days

Secondary Outcomes

  • 3-year disease free survival(36 months)

Study Sites (1)

Loading locations...

Similar Trials