Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
NCT07482566

Proximal Versus Total Gastrectomy for Locally Advanced Siewert Type II-III Gastroesophageal Junction Cancer

Led by Nurettin Şahin · Updated on 2026-03-20

120

Participants Needed

1

Research Sites

365 weeks

Total Duration

On this page

Sponsors

N

Nurettin Şahin

Lead Sponsor

A

Ankara City Hospital Bilkent

Collaborating Sponsor

AI-Summary

What this Trial Is About

This multicenter prospective randomized clinical trial aims to compare the safety and oncological effectiveness of proximal gastrectomy and total gastrectomy in patients with locally advanced Siewert type II-III gastroesophageal junction cancer. Eligible patients will be randomly assigned to undergo either proximal gastrectomy or total gastrectomy using open, laparoscopic, or robotic surgical approaches according to clinical suitability. The primary outcome of the study is 3-year disease-free survival. Secondary outcomes include postoperative mortality, postoperative complications, and the number of metastatic lymph nodes retrieved. Patients will be followed for up to five years after surgery to evaluate long-term oncological outcomes.

CONDITIONS

Official Title

Proximal Versus Total Gastrectomy for Locally Advanced Siewert Type II-III Gastroesophageal Junction Cancer

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 90 years
  • Histologically confirmed locally advanced Siewert type II-III gastroesophageal junction cancer
  • Considered operable after multidisciplinary tumor board evaluation
  • Candidate for curative surgical resection with D2 lymphadenectomy
  • Provision of written informed consent
Not Eligible

You will not qualify if you...

  • Early-stage gastroesophageal junction cancer
  • Gastric cancers located in the antrum or corpus
  • Severe anesthetic risk (American Society of Anesthesiologists [ASA] class IV or higher)
  • Pregnancy
  • Patients unwilling or unable to provide informed consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

Bakirkoy Dr. Sadi Konuk Training and Research Hospital

Istanbul, Istanbul, Turkey (Türkiye), 34147

Actively Recruiting

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Research Team

T

Turgut Donmez, MD

CONTACT

T

Tolga Dinc, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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