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Clinical Trials/NCT04153058
NCT04153058
Enrolling By Invitation
Not Applicable

Randomized Controlled Trials on Clinical Outcomes of Robotic Versus Laparoscopic Assisted Radical Gastrectomy for Advanced Siewert II/III Esophagogastric Junction Adenocarcinoma

Fujian Medical University1 site in 1 country300 target enrollmentNovember 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Esophagogastric Junction Adenocarcinoma
Sponsor
Fujian Medical University
Enrollment
300
Locations
1
Primary Endpoint
3-year disease free survival rate
Status
Enrolling By Invitation
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to explore the clinical outcomes of the robotic assisted radical gastrectomy for advanced Siewert II/III esophagogastric junction adenocarcinoma(cT2-4a, N-/+, M0)

Detailed Description

In recent years, the incidence of gastric cancer has been decreasing year by year in the world, but the incidence of adenocarcinoma of the esophagogastric junction (AEG) has shown a significant upward trend, especially in Western countries such as Europe and the United States. The prognosis of AEG is poor, therefore, it is extremely necessary to establish AEG's best diagnosis and treatment strategies to improve the long-term outcome of AEG. Robotic surgery has been developed with the aim of improving surgical quality and overcoming the limitations of conventional laparoscopy in the performance of complex mini-invasive procedures. The study is designed to explore the clinical outcomes of the robotic assisted radical gastrectomy for advanced Siewert II/III esophagogastric junction adenocarcinoma (cT2-4a, N-/+, M0) by comparing with laparoscopic assisted.

Registry
clinicaltrials.gov
Start Date
November 1, 2019
End Date
October 2025
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fujian Medical University
Responsible Party
Principal Investigator
Principal Investigator

Chang-Ming Huang, Prof.

Professor

Fujian Medical University

Eligibility Criteria

Inclusion Criteria

  • Age from over 18 to under 75 years
  • Primary gastric adenocarcinoma (papillary, tubular, mucinous, signet ring cell, or poorly differentiated) confirmed pathologically by endoscopic biopsy
  • cT2-4a(clinical stage tumor), N-/+, M0 at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual 8th Edition
  • Expected to perform total gastrectomy with D2+No.19+No.20 lymph node dissction to obtain R0 resection sugicall results.
  • Performance status of 0 or 1 on ECOG (Eastern Cooperative Oncology Group) scale
  • ASA (American Society of Anesthesiology) class I to III
  • Written informed consent

Exclusion Criteria

  • Women during pregnancy or breast-feeding
  • Severe mental disorder
  • History of previous upper abdominal surgery (except laparoscopic cholecystectomy)
  • History of previous gastric surgery (except ESD/EMR (Endoscopic Submucosal Dissection/Endoscopic Mucosal Resection )for gastric cancer)
  • Gastric multiple primary carcinoma
  • Enlarged or bulky regional lymph node (diameter over 3cm)supported by preoperative imaging
  • History of other malignant disease within the past 5 years
  • History of previous neoadjuvant chemotherapy or radiotherapy
  • History of unstable angina or myocardial infarction within the past 6 months
  • History of cerebrovascular accident within the past 6 months

Outcomes

Primary Outcomes

3-year disease free survival rate

Time Frame: 36 months

3-year disease free survival rate

Secondary Outcomes

  • 3-year overall survival rate(36 months)
  • 3-year recurrence pattern(36 months)
  • Time to first ambulation(30 days)
  • The amount of abdominal drainageare(30 days)
  • intraoperative morbidity rates(1 day)
  • overall postoperative serious morbidity rates(30 days)
  • Duration of hospital stay(30 days)
  • overall postoperative morbidity rates(30 days)
  • Time to soft diet(30 days)
  • number of retrieved lymph nodes(14 days)
  • Time to first liquid diet(30 days)
  • Time to first flatus(30 days)
  • Hospitalization costs(30 days)
  • postoperative nutritional status(3, 6, 9 and 12 months)

Study Sites (1)

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