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A Phase III Study Comparing Total and Partial Omentectomy for Patients With Advanced Gastric Cancer

T

Tianjin Medical University

Status

Enrolling

Conditions

Gastric Cancer

Treatments

Procedure: Type of omentectomy

Study type

Interventional

Funder types

Other

Identifiers

NCT04843215
E20210171

Details and patient eligibility

About

This is a phase III, multicenter, prospective, randomized, controlled clinical trial to evaluate the impact of omentectomy for advanced gastric cancer on patient survival.

Full description

In order to evaluate the impact of omentectomy for advanced gastric cancer on patient survival, we designed this trial. Patients who received curative gastrectomy were divided into two groups based on whether they underwent omentectomy. The purpose of this study is to prove the non-inferiority of omentum preservation compared with omentectomy in patients with T3-T4a gastric cancer.

Enrollment

950 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Had been treated with Radical resection (D2, R0) of gastric cancer (Lymph node≥16);

  2. Physical condition and organ function allows to tolerable abdominal surgery;

  3. Willing and able to comply with the program during the study period;

  4. Written informed consent provided;

  5. ≥ 18 and ≤ 70 years of age; preoperative gastric cancer patients with pathologically confirmed;

  6. With more than a 6-month life expectancy;

  7. No other serious concomitant diseases; Sufficient organ functions;

  8. No previous history of chemotherapy or radiotherapy;

  9. All patients accept 8 cycles XELOX chemotherapy regimen;

  10. Clinical stage: T3-4aN0-+M0; 11 . Macroscopic types :Borrmann I-III;

  11. Not greater curvature tumor; with distal or total gastrectomy; 13. No previous surgery for any abdominal disease, except an appendectomy for appendicitis, a laparoscopic cholecystectomy for gallbladder stones; No previous history of peritonitis, pancreatitis; 14. Karnofsky performance status (KPS)>60; Eastern Cooperative Oncology Group Performance Status (ECOG): 0-1.

Exclusion criteria

Pregnancy or breast feeding; 2. Patients with Serious liver disease (such as cirrhosis, etc.), kidney disease, respiratory disease or uncontrolled diabetes, hypertension and other chronic systemic diseases, heart disease with Clinical symptoms, such as congestive heart failure, coronary heart disease symptoms, drug is difficult to control arrhythmia, hypertension, or six months had a myocardial infarction attack, or cardiac insufficiency; 3. Organ transplantation patients need immunosuppressive therapy; 4. Severe recurrent infections were not controlled or with other serious concomitant diseases; 5. Patients got other primary malignant tumors (except curable skin basal cell carcinoma and cervical cancer in situ) except gastric cancer within 5 years; 6. Psychiatric disease which require treatment; 7. Have the history of organ transplantation; 8. Within 6 months before study starts and in the process of this study, patients participate in other clinical researches. 9. Advanced gastric cancer with omentum invasion 10. Patients can't treated with XELOX after surgery; 11 . Macroscopic types : Borrmann IV; 12. Tumor invasion of adjacent organ (T4b) or with distant metastasis#M1 #; 13. Tumor invasion the greater curvature invasion.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

950 participants in 2 patient groups

Experimental group/D2 radical gastrectomy with partial omentectomy
Experimental group
Description:
Partial omentectomy with preservation of the greater omentum at \>3 cm from the gastroepiploic arcade.
Treatment:
Procedure: Type of omentectomy
Control group/D2 radical gastrectomy with total omentectom
No Intervention group
Description:
Control group with total omentectomy

Trial contacts and locations

1

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Central trial contact

Han Liang, Master; Bik Ke, Doctor

Data sourced from clinicaltrials.gov

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