Adenocarcinoma of the Esophagogastric Junction

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Review clinical trials related to Adenocarcinoma of the Esophagogastric Junction. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Sino-Russian Comparison of Outcomes After Proximal Gastrectomy With Double-Tract Reconstruction

This two-center retrospective observational cohort study compares Chinese and Russian patients who underwent curative proximal gastrectomy with double-tract reconstruction for proximal gastric adenocarcinoma or Siewert type II/III adenocarcinoma of the esophagogastric junction. The study evaluates postoperative reflux, nutritional status, perioperative outcomes, complications, and long-term survival. Propensity score matching will be used to improve comparability between the two cohorts.

Participants needed: 250
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: The First Affiliated Hospital with Nanjing Medical UniversityUpdated: Sep 2, 2026Locations: 2
Eligibility criteria

Age 18 to 75 years. [+5]

Previous gastric or esophageal surgery, except limited endoscopic treatment such... [+4]

Status: Not yet recruiting

Intraoperative Margin Techniques for Esophagogastric Junction Adenocarcinoma: A Controlled Study

The goal of this clinical trial is to learn if the EndoScell Scanner (ES) imaging system can accurately assess tumor-free surgical margins during surgery for adenocarcinoma of the esophagogastric junction (AEG), compared with standard frozen-section pathology. The main questions it aims to answer are: * Is ES non-inferior to intraoperative frozen-section pathology in identifying positive or negative tumor margins? * Does ES shorten the time needed for margin assessment and reduce the number of additional tissue resections required? Researchers will compare an ES-assisted surgical arm with a conventional frozen-section arm to see if ES improves margin accuracy, shortens operative time, and increases the rate of complete (R0) tumor removal. Participants will * undergo standard AEG resection with randomized assignment to either ES or frozen-section margin checks; * allow collection of margin tissue samples for ES, frozen-section, and final paraffin pathology; * attend routine follow-up visits for up to 2 years to monitor for local recurrence.

Participants needed: 314
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Fudan UniversityUpdated: Jul 31, 2025
Eligibility criteria

Plan to receive surgical resection of AEG; [+1]

Patients who are allergic to methylene blue and fluorescein sodium; [+6]