Application of a New Surgical Technique in Proximal Gastrectomy: a Prospective, Multicenter Randomized Controlled Study

July 20, 2025 updated by: Hao Hankun, Huashan Hospital

Application of Hao's Esophagogastrostomy by Fissure Technique: a Prospective, Multicenter Randomized Controlled Study

This is a prospective study using a multicenter, randomized, controlled, open label, and efficacy validated approach.At present, there is no universally recognized optimal method for gastrointestinal reconstruction after proximal gastrectomy in the surgical treatment of gastric cancer.Author's team has proposed an innovative method named Hao's Esophagogastrostomay by Fisture Technique (HEFT).By adding anti reflux structures such as "false gastric fundus" and "false cardia" to the anastomosis of the residual stomach of the esophagus, not only can the purpose of anti reflux be achieved, but also the normal physiological channel can be maintained, it can fully utilize residual stomach function and reduce the difficulty of surgery.Through retrospective research, our single center has confirmed that HEFT is safe and feasible.On this basis, this study will compare the nutritional status, short- and medium- to long-term safety after laparoscopic HEFT and double-tract reconstruction , in order to evaluate and discover more reasonable digestive tract reconstruction methods after proximal gastrectomy, and to promote the development and popularization of minimally treatment technology for gastric cancer.

This study was jointly conducted by Shanghai-level hospitals (Huashan Hospital ,Shanghai Cancer Center, and Ruijin Hospital), with Huashan Hospital as the leading unit. This study will recruit 52 patients, with 26 patients in the experimental group and 26 patients in the control group. Using a central dynamic randomization method based on minimization, patients are assigned to groups in a 1:1 ratio. Based on the different anastomotic methods used in proximal gastrectomy, patients are divided into a HEFT group (experimental group) and a double-tract reconstruction group (control group).Plan to collect cases for 2 years, and follow up for another year after the last case is enrolled.

The primary endpoint of the study was the body weight loss (BWL) rate at 1 year after surgery. Secondary endpoints: Effect evaluation indicators: hemoglobin level at 1 year after surgery; Serum albumin level at 1 year after surgery; The incidence of anastomotic stenosis 1 year after surgery; Incidence of reflux esophagitis at 1 year after surgery. Evaluation of short-term surgical safety (duration: 7 days): operation time, intraoperative bleeding, anastomotic leakage, pancreatic leakage, and incidence of abdominal infection; Evaluation of medium- and long-term safety after surgery (duration: 36 months): overall survival rate at 3 years after surgery; disease-free survival rate at 3 years after surgery.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

52

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Shanghai, China
        • Recruiting
        • Huashan Hospital, Fudan University
        • Contact:
      • Shanghai, China, 200025
        • Recruiting
        • Department of General Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
        • Contact:
      • Shanghai, China
        • Recruiting
        • Second Department of Gastric Surgery, Fudan University Shanghai Cancer Center,
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. 18 years old ≤ 80 years old;
  2. The primary tumor lesion is located in the upper part of the stomach or the esophagogastric junction (Siewert II or III), and it is expected that R0 surgical results can be obtained by performing proximal gastrectomy and D2 dissection;
  3. The primary lesion was diagnosed as adenocarcinoma through endoscopic biopsy and histopathological examination;
  4. If it is upper gastric adenocarcinoma, the clinical TNM staging based on imaging needs to be cT1N0M0. If it is ductal gastric junction adenocarcinoma, it needs to be cT1-3N0-1M0, and clinical imaging judgment shows no distant gastric lymph node metastasis;
  5. Expected survival exceeds 6 months;
  6. No history of upper abdominal surgery (excluding laparoscopic cholecystectomy);
  7. No chemotherapy, radiotherapy, targeted therapy, immunotherapy, etc. were performed before surgery;
  8. Preoperative ECOG (Eastern Cooperative Oncology Group) physical status score 0/1;
  9. Preoperative ASA (American Society of Anesthesiologists) grading I-III ;
  10. Good function of important organs;
  11. Sign the patient's informed consent form

Exclusion Criteria:

  1. Preoperative imaging examination suggests the fusion of enlarged lymph nodes (maximum diameter ≥ 3cm) in the area;
  2. Pregnant and lactating women;
  3. Suffering from other malignant tumors within 5 years;
  4. Preoperative body temperature ≥ 38 ℃ or complicated with infectious diseases requiring systematic treatment;
  5. Serious mental illness;
  6. Severe respiratory diseases, FEV1<50% of the expected value;
  7. Severe liver and kidney dysfunction;
  8. History of unstable angina or heart attack within 6 months;
  9. History of cerebral infarction or cerebral hemorrhage within 6 months, excluding old intracavitary infarction;
  10. Apply systemic corticosteroid therapy within one month;
  11. Patients with complications of gastric cancer (bleeding, perforation, obstruction) requiring emergency surgery;
  12. The patient has participated or is currently participating in other clinical studies (within 6 months)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Performing Hao's esophagogastrostomy by fissure technique
This is an innovative surgical method applied in proximal gastrectomy. By adding anti reflux structures such as "false gastric fundus" and "false cardia" on the basis of esophageal residual gastric anastomosis, the goal of anti reflux is achieved, while maintaining normal physiological channels and fully utilizing residual gastric function, reducing the difficulty of proximal gastrectomy surgery
Active Comparator: Performing double-tract reconstruction
This is a traditional surgical method that has been widely used in proximal gastrectomy. After disconnecting the proximal stomach, performing Roux-en-Y anastomosis of the esophagus and jejunum firstly, followed by lateral anastomosis of the residual stomach and jejunum. Previous studies have confirmed its safety and effectiveness, but there are also issues of gastric channel disuse and high missed detection rate of residual stomach.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
body weight loss(BWL)
Time Frame: From enrollment to 1 year after surgery
Measure the weight before surgery and 1 year after surgery, BWL=(preoperative weight -1 year after surgery weight)/preoperative weight (unit:%)
From enrollment to 1 year after surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hemoglobin 1 year after surgery
Time Frame: 1 year after surgery
Hemoglobin (unit: g/L) 1 year after surgery will be used to evaluate operation effect.
1 year after surgery
Serum albumin 1 year after surgery
Time Frame: 1 year after surgery
Serum albumin (unit: g/L) 1 year after surgery will be used to evaluate operation effect.
1 year after surgery
Incidence of anastomotic stenosis 1 year after surgery
Time Frame: 1 year after surgery
Incidence of anastomotic stenosis(%) 1 year after surgery will be used to evaluate operation effect.
1 year after surgery
Incidence of reflux esophagitis 1 year after surgery
Time Frame: 1 year after surgery
Incidence of reflux esophagitis 1 year after surgery will be used to evaluate operation effect.
1 year after surgery
Duration of surgery
Time Frame: intraoperative
Time spent on the whole operation(minutes)will be used to evaluate short-term safety of the surgery
intraoperative
Intraoperative blood loss
Time Frame: Intraoperative
Intraoperative blood loss(ml) will be used to evalute short-term safety of the surgery.
Intraoperative
Incidence of anastomotic leakage 7 days after surgery
Time Frame: 7 days after surgery
Incidence of anastomotic leakage(%) 7 days after surgery will be used to evaluate short-term safety of the surgery
7 days after surgery
Incidence of pancreatic leakage 7 days after surgery
Time Frame: 7 days after surgery
Incidence of pancreatic leakage 7 days after surgery will be used to evaluate short-term safety of the surgery.
7 days after surgery
Incidence of abdominal infection 7 days after surgery
Time Frame: 7 days after surgery
Incidence of abdominal infection 7 days after surgery will be used to evaluate short-term safety of the surgery.
7 days after surgery
Overall survival (OS) 3 years after surgery
Time Frame: 3 years after surgery
Overall survival (OS, %) 3 years after surgery will be used to evaluate medium- and long-term postoperative safety
3 years after surgery
Disease free survival (DFS) 3 years after surgery
Time Frame: 3 years after surgery
Disease free survival (DFS, %) 3 years after surgery will be used to evaluate medium- and long-term postoperative safety,
3 years after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 4, 2024

Primary Completion (Estimated)

June 1, 2029

Study Completion (Estimated)

June 1, 2029

Study Registration Dates

First Submitted

November 5, 2024

First Submitted That Met QC Criteria

November 6, 2024

First Posted (Actual)

November 7, 2024

Study Record Updates

Last Update Posted (Actual)

July 22, 2025

Last Update Submitted That Met QC Criteria

July 20, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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