Preliminary Efficacy Analysis of "C" Single Flap Plasty Reconstruction After Laparoscopic Proximal Gastrectomy
Launched by DAORONG WANG · Dec 17, 2024
Trial Information
Current as of June 26, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at a new surgical method called "C" Single Flap Plasty Reconstruction for patients with early-stage gastric cancer, specifically in the upper part of the stomach. The goal is to see if this new approach can effectively treat cancer while also helping to prevent issues like reflux, which can happen after surgery. The trial will involve patients aged 18 to 80 who have been diagnosed with certain types of stomach cancer and meet specific health criteria.
To be part of this study, participants must not have any distant spread of cancer and should not have specific health conditions that could complicate surgery. If eligible, patients can expect to undergo the "C" reconstruction procedure along with standard care for their cancer. Before joining, patients and their families will need to provide consent, ensuring they understand what the study involves. This trial represents an important step in finding better surgical options for patients with gastric cancer, aiming to improve both treatment outcomes and quality of life.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Age between 18-80 years old, male or female;
- • 2. Pathological diagnosis of preoperative endoscopic biopsy: the tumor is located in the upper 1/3 of the stomach (including the esophagogastric junction), and the clinical staging of gastric cancer: Ia and Ib (T1N0M0, T1N1M0, and T2N0M0) according to the eighth edition of the AJCC ;
- • 3. No distant metastasis was observed on preoperative chest radiograph, abdominal ultrasound, or upper abdominal CT;
- • 4. ASA grade 1-3;
- • 5. Patients without contraindications to surgery;
- • 6. Patients and their families voluntarily signed the informed consent form and participated in the study;
- Exclusion Criteria:
- • 1. Patients diagnosed with primary tumors or distant metastasis;
- • 2. Patients whose tumor is located in the greater curvature side of the stomach;
- • 3. Patients with coagulation dysfunction that could not be corrected;
- • 4. Patients who were diagnosed with viral hepatitis and cirrhosis;
- • 5. Patients who were diagnosed with diabetes mellitus, uncontrolled or controlled with insulin;
- • 6. Patients with organ failure such as heart, lung, liver, brain, and kidney failure;
- • 7. Patients with ascites or cachexia preoperatively in poor general conditions;
- • 8. Patients diagnosed with immunodeficiency, immunosuppression, or autoimmune diseases (such as allogeneic bone marrow transplant, immunosuppressive drugs, SLE, etc.).
- • 9. Patients refusing to sign the informed consent of the study;
About Daorong Wang
Daorong Wang is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through rigorous scientific inquiry. With a strong focus on innovative therapeutic approaches, Daorong Wang leads and manages clinical trials that adhere to the highest ethical and regulatory standards. By fostering collaboration among multidisciplinary teams, the organization aims to accelerate the development of groundbreaking treatments while ensuring participant safety and data integrity. Daorong Wang's mission is to contribute significantly to the evolving landscape of healthcare, ultimately enhancing the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Yangzhou, Jiangsu, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported