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NCT07635836Recruiting

Comparison of Double-tract and Tubular Gastric Anastomosis in Proximal Gastric Cancer

Comparison of Gastroesophageal Reflux and Quality of Life Between Double-tract and Tubular Gastric Anastomosis in Proximal Gastric Cancer Patients

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Brief summary (registry, in English)

This study includes patients diagnosed with proximal gastric cancer (Siewert type II/III, cT1-3N0-1M0) across six tertiary hospitals, who underwent either double-tract reconstruction (DTR) or tubular gastric anastomosis (TGA). Participants were divided into two groups based on the surgical procedure. We conducted a comparative analysis of postoperative outcomes by evaluating electronic medical records, postoperative gastroscopy, 24-hour esophageal pH monitoring, and relevant rating scales.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
52 (estimated)
First submitted
3 Jun 2026
Start date
1 May 2026
Primary completion date
1 May 2027
Lead sponsor
Qilu Hospital of Shandong University
NCT number
NCT07635836

What you commit to

  • Study type: Interventional
  • Planned participants: 52
  • From 1 May 2026 to the primary completion date, 1 May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of prior upper abdominal surgery, gastrointestinal malformation, or psychiatric disorders

Other illness

  • Presence of other malignant tumors or severe chronic diseases (e.g., severe diabetes mellitus, chronic kidney disease, decompensated cirrhosis, etc.)
  • Preoperative diagnosis of obstructive motor disorders of the cardia (including achalasia spectrum disorders)

Lab values

  • Severe preoperative malnutrition (albumin \<30 g/L, prealbumin \<150 mg/L)

Other

  • Preoperative endoscopic diagnosis of Barrett's esophagus
  • Inability to cooperate with or complete the required postoperative examinations

Who the study is looking for

  • Pathologically confirmed gastric adenocarcinoma by biopsy
  • Carcinoma of the upper gastric body or Siewert type II/III adenocarcinoma of the esophagogastric junction (AEG), with a clinical stage of cT1-3N0-1M0
  • Age 18-75 years, with a performance status (PS) score of 0-2
  • Candidates for planned surgical resection, eligible for either double-tract reconstruction or tubular gastric anastomosis based on preoperative assessment
  • No severe dysfunction of vital organs (liver, kidney, heart, lung, or brain), and no severe infection or uncontrolled chronic diseases

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Qilu Hospital of Shandong University
Coordinator of this site? Confirm its status
JinanChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.