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Recruiting NCT05537129

Laparoscopic vs Open Total Gastrectomy for Gastric Cancer

No phase Interventional Gastric Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Total Gastrectomy.
Who it may be relevant to
Registry conditions: Gastric Cancer. Basic parameters: 20 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Prospective, Multicentral, Open-label, Randomized, Controlled Clinical Trial to Compare the Survival, Morbidity and Mortality of Laparoscopic and Open Total Gastrectomy for Gastric Cancer

Overview

The aim of the present study is to demonstrated the the safety and feasibility of laparoscopic total gastrectomy comparing with open total gastrectomy.

Detailed description

Gastric cancer is most common cause of cancer-related deaths in the world. Laparoscopic distal gastrectomy has been demonstrated to be safe and effective compared with open distal gastrectomy. With an increase in incidences of proximal gastric cancer over the last decades, total gastrectomy has been prefered by surgeons, and laparoscopic total gastrectomy has become the alternative option. However, the safety and feasibility of laparoscopic total gastrectomy have yet to be proved completely.

Interventions

  • Procedure Total Gastrectomy
    The laparoscopic or open total gastrectomy with D2 lymphadenectomy was performed according to the Japanese gastric cancer treatment guidelines.

Primary outcome measures

  • 3 year-DFS [Time frame: 3 year]
Secondary outcome measures (2)
  • 3 year-OS [Time frame: 3 year]
  • morbidity and mortality rates [Time frame: 30 days following surgeries]

Eligibility criteria

Inclusion criteria

  • histologically proven gastric adenocarcinoma in the upper or middle third of the stomach (by preoperative gastrofiberscopy)
  • age between 20 and 80 years old
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • clinical stage I-III (T1-4aN0-2M0) according to the 8th edition of the Americal Joint Committee on Cancer System (Clinical stage was determined based on the finding of gastrofiberscopy and abdominal computed tomography)
  • scheduled for total gastrectomy with D2 lymphadenectomy, and possible for R0 surgery by this procedures (Lymphadenectomy is performed on the basis of the criteria of the Japanese
  • written informed consent
  • without preoperative chemotherapy and radiotherapy

Exclusion criteria

  • clinical stage T1-4N3M0 or T4bN0-3M0 according to the 8th edition of the Americal Joint Committee on Cancer System
  • history of chemotherapy, radiotherapy, immunotherapy or target therapy
  • perigastric lymphnode≥3cm
  • received gastric surgery (i.e. gastrectomy or gastrojejunostomy)
  • multiple primary tumors
  • suffering from other serious diseases, including cardiovascular, respiratory, kidney, or liver disease, complicated by poorly controlled hypertension, diabetes, mental disorders or diseases.
  • patients need emergency operation with complication of gastric cancer
  • adhesion due to the previous intraabdominal surgery
  • need for combined organ resection due to aggression of gastric cancer of other disease,
  • vulnerable people who cannot communicate or are pregnant (or planning to be pregnant)
  • currently participating or participated in other clinical trials in the last 6 months

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

China · 1 center
  • Fudan University Shanghai Cancer Center — Shanghai

Identifiers

NCT: NCT05537129 · LOTGGC

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗