A Trial to Evaluate the Superior Mesenteric Vein (14V) Lymphadenectomy for Distal Advanced Gastric Cancer

NCT02272894 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 510

Last updated 2015-12-09

No results posted yet for this study

Summary

This trial is going to evaluate the advantage of D2 radical gastrectomy plus 14v lymph node dissection in 3-year survival rates of advanced gastric cancers.

Conditions

Interventions

PROCEDURE

Dissection of the Superior Mesenteric Vein Lymph Node

14v lymph node dissection

Sponsors & Collaborators

  • The First Affiliated Hospital with Nanjing Medical University

    collaborator OTHER
  • Shanxi Province Cancer Hospital

    collaborator OTHER
  • Peking University Cancer Hospital & Institute

    collaborator OTHER
  • Qingdao University

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Sun Yat-sen University

    collaborator OTHER
  • Harbin Medical University

    collaborator OTHER
  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences

    collaborator OTHER
  • The First Affiliated Hospital of Dalian Medical University

    collaborator OTHER
  • Qinghai University

    collaborator OTHER
  • Second Hospital of Jilin University

    collaborator OTHER
  • The First Affiliated Hospital of Zhengzhou University

    collaborator OTHER
  • Wulumuqi General Hospital of Lanzhou Military Command

    collaborator OTHER
  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • Nanjing PLA General Hospital

    collaborator OTHER
  • Tianjin Medical University Cancer Institute and Hospital

    lead OTHER

Principal Investigators

  • Han Liang, Master · Tianjin Medical University Cancer Hospital

Eligibility

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

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2016-11-30
Completion
2016-12-31

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 NCT02272894 on ClinicalTrials.gov