Study on Laparoscopic Spleen-Preserving No. 10 Lymph Node Dissection for Advanced Gastric Cancer

NCT02845986 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 251

Last updated 2020-02-05

No results posted yet for this study

Summary

The purpose of this study is to explore the safety and feasibility of the Laparoscopic Spleen-Preserving No. 10 Lymph Node Dissection for patients with locally advanced upper third gastric adenocarcinoma(cT2-4a, N-/+, M0).

Conditions

  • Stomach Neoplasms

Interventions

PROCEDURE

Laparoscopic Spleen-Preserving No.10 Lymph Node Dissections

After exclusion of T4b, bulky lymph nodes, or distant metastasis case et al. Laparoscopic spleen-preserving No.10 lymph node dissections will be performed with curative treated intent in patients with locally advanced upper third gastric adenocarcinoma.

DRUG

oxaliplatin

oxaliplatin or platinum-based chemotherapy is used when the patients undergo adjuvant chemotherapy after the surgery.

Sponsors & Collaborators

  • Peking University Cancer Hospital & Institute

    collaborator OTHER
  • Southwest Hospital, China

    collaborator OTHER
  • Fujian Provincial Hospital

    collaborator OTHER
  • Zhangzhou Municipal Hospital of Fujian Province

    collaborator OTHER
  • Shanghai Zhongshan Hospital

    collaborator OTHER
  • Meizhou People's Hospital

    collaborator OTHER
  • Guangdong Provincial People's Hospital

    collaborator OTHER
  • Guangdong Provincial Hospital of Traditional Chinese Medicine

    collaborator OTHER
  • Second Hospital of Jilin University

    collaborator OTHER
  • The First Affiliated Hospital with Nanjing Medical University

    collaborator OTHER
  • Nanfang Hospital, Southern Medical University

    collaborator OTHER
  • Affiliated Hospital of Qinghai University

    collaborator OTHER
  • The First Affiliated Hospital of Xiamen University

    collaborator OTHER
  • RenJi Hospital

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • First Affiliated Hospital Xi'an Jiaotong University

    collaborator OTHER
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • The First Hospital of Putian City, Putian, Fujian

    collaborator OTHER_GOV
  • Longyan City First Hospital

    collaborator OTHER
  • Fujian Medical University

    lead OTHER

Principal Investigators

  • Changming Huang, Professor · Fujian Medical University Union Hospital,China

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-09-01
Primary Completion
2017-10-12
Completion
2020-10-12

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02845986 on ClinicalTrials.gov