Status:

UNKNOWN

Length of the Proximal Resection Margin for Siewert-II/Siewert-III Tumors

Lead Sponsor:

West China Hospital

Conditions:

Stomach Neoplasms

Siewert Type II Adenocarcinoma of Esophagogastric Junction

Eligibility:

All Genders

18-75 years

Phase:

NA

Brief Summary

The incidence of adenocarcinomas of the esophagogastric junction (AEJ) has increased rapidly during the past decades. By the Siewert classification, the AEJ is the tumor center located 5 cm above the ...

Detailed Description

Standard Operating Procedure (SOP) 1. Preoperative evaluation Patients satisfied with inclusion/exclusion criteria will be informed to join in the clinical study and signature the inform consent. 2. ...

Eligibility Criteria

Inclusion

  • Preoperative endoscopy and biopsy confirmed upper third gastric adenocarcinoma (Siewert-II/Siewert-III), and predictively feasible of radical total gastrectomy;
  • Predictively resectable diseases, advanced gastric cancer, of preoperative staging JGCA 14th Edition cT2N0M0-T4aN3bM0, Ib-IIIc stage;
  • Age:≤75 years, or ≥18 years;
  • Without serious disease and malignance disease;
  • WHO performance score ≤2, ASA score ≤3;
  • No limit to sexual and race;
  • Informed consent required.

Exclusion

  • Patients with other severe complications cannot tolerate surgery: such as severe heart and lung diseases, heart function below clinical stage 2, uncontrollable hypertension, pulmonary infection, moderate to severe COPD, chronic bronchitis, severe diabetes and / or renal insufficiency, severe hepatitis and / or function below the rank of CHILD B grade, and severe malnutrition, etc;
  • Patients treated with neoadjuvant chemotherapy or radiation therapy which might affect the efficacy observation;
  • Severity mental diseases;
  • Primary lesion cannot be resected in the pattern of transabdominal proximal gastrectomy, but for total gastrectomy, Whipple's procedure, or combined organ resection or with a transthoracic approach surgery;
  • After signature the Clinical trial agreement, patients and their agent will quit the trial.

Key Trial Info

Start Date :

January 1 2015

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 1 2023

Estimated Enrollment :

320 Patients enrolled

Trial Details

Trial ID

NCT02313688

Start Date

January 1 2015

End Date

December 1 2023

Last Update

December 11 2017

Active Locations (1)

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1

West China Hospital

Chengdu, Sichuan, China, 610041