Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT07183150

The Possible Range of No.4sb Lymph Node Dissection of Locally Advanced Distal Gastric Cancer

Led by Tianjin Medical University Cancer Institute and Hospital · Updated on 2025-09-19

400

Participants Needed

1

Research Sites

123 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The main purpose of this study is to evaluate the reasonable range of No.4sb lymph node dissection of locally advanced distal gastric cancer.

CONDITIONS

Official Title

The Possible Range of No.4sb Lymph Node Dissection of Locally Advanced Distal Gastric Cancer

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Between 18 and 75 years of age
  • Pathologically confirmed gastric cancer before surgery
  • Treated with radical resection (D2, R0) of gastric cancer with 16 or more lymph nodes removed
  • Willing and able to follow the study program
  • Physical condition and organ function allow toleration of abdominal surgery
  • Provided written informed consent
  • Undergoing radical laparoscopic distal subtotal gastrectomy
  • Life expectancy of more than 6 months
  • No other serious concomitant diseases
  • Sufficient organ functions
  • No history of chemotherapy or radiotherapy
  • Clinical stage T2-4aNxM0
  • Karnofsky performance status (KPS) greater than 60
  • Eastern Cooperative Oncology Group performance status (ECOG) 0-1
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding
  • Serious liver disease such as cirrhosis
  • Serious kidney disease
  • Serious respiratory disease
  • Uncontrolled diabetes or hypertension
  • Heart disease with clinical symptoms such as congestive heart failure or coronary heart disease
  • Difficult to control arrhythmia or hypertension
  • Recent myocardial infarction within 6 months
  • Cardiac insufficiency
  • Organ transplant patients needing immunosuppressive therapy
  • Severe recurrent infections not controlled
  • Other serious concomitant diseases
  • Other primary malignant tumors within 5 years except curable skin basal cell carcinoma and cervical cancer in situ
  • Psychiatric disease requiring treatment
  • History of organ transplantation
  • Participation in other clinical research within 6 months before or during the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Tianjin Medical University Cancer Hospital

Tianjin, Tianjin Municipality, China, 300060

Actively Recruiting

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Research Team

B

Bin Ke, MD.

CONTACT

P

Peng Ru Zhang, MD.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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