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Recruiting Not applicable

Omentum Preservation Versus Complete Omentectomy in Gastrectomy for Gastric Cancer

NCT05180864 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2024-03-01
Last updated
2025-09-04

Condition(s) studied

Stomach Neoplasm

Investigational drug(s) / intervention(s)

Gastrectomy

Gastrectomy: Open or minimally invasive (sub)total gastrectomy

Study summary

Curative therapy for gastric cancer usually consists of perioperative chemotherapy and a radical (R0) gastrectomy. A radical resection includes a modified D2 lymphadenectomy, and, generally, a complete omentectomy, to ensure the removal of omental metastatic lymph nodes and tumor deposits.

The omentum has some essential functions within the peritoneal cavity. The omentum functions as regulator of regional immune responses to prevent infections and, additionally, it prevents adhesions that can lead to small bowel obstruction. Omentectomy is associated with increased incidence of early and late postoperative complications such as abdominal abscess, ileus, and wound infections in various types of surgery.

There is little evidence regarding survival benefit of routine complete omentectomy during gastrectomy. The investigators hypothesize that omitting a complete omentectomy (and instead preserve the greater omentum distal of the gastroepiploic arcade) during gastrectomy for cancer does not negatively impact survival.

OMEGA is a randomized controlled, open, parallel, non-inferiority, multicenter trial. Adult patients (\>18 years) with primary resectable gastric cancer, clinical stage T2-4a N0-3 M0 or cT1N+ scheduled for open or minimally invasive (sub)total gastrectomy are included. The primary study objective is to investigate whether omentum preservation in gastrectomy for cancer is non-inferior to complete omentectomy in terms of three-year overall survival.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion criteria * Primary resectable gastric adenocarcinoma, clinical stage T1-4aN0-3M0 * ASA 1-3 (able to undergo surgery) * Scheduled for open or minimally invasive (sub)total gastrectomy with modified D2-lymphadenectomy, with or without perioperative chemotherapy * Age above 18 * Able to complete questionnaires in Dutch, English or Italian * Written informed consent * Esophageal invasion \< 2 cm defined from the upper margin of the gastric rugae as determined by endoscopy Exclusion Criteria: * Gastric cancer clinically staged as T1N0 * Locally advanced gastric cancer requiring multi-visceral resection * Pregnancy * Previous malignancy (excluding non-melanoma skin cancer, pancreatic neuroendocrine tumor (pNET) \<2cm, and gastrointestinal stromal tumor (GIST) \<2cm), unless no evidence of disease and diagnosed more than three years before diagnosis of gastric cancer, or with a life expectancy of more than five years from date of inclusion * Serious concomitant systemic disorders that would compromise the safety of the patient or his/her ability to complete the study, at the discretion of the investigator * Previous gastric or omental surgery, with the exclusion of a gastric perforation Indication for thoracotomy/thoracoscopy

Primary outcome measure(s)

  • Overall survival — 3 years after surgery
    Overall survival is defined as the period of time from operation to death from any cause. Patients alive and free of all these events will be censored at the last follow-up

Trial sites (16)

FacilityCityRegionStatus
University Medical Center of the Johannes Gutenberg University Mainz Germany Not Yet Recruiting
Azienda Ospedaliera Universitaria Siena Italy Not Yet Recruiting
Amsterdam UMC Amsterdam North Holland Recruiting
Ziekenhuis Groep Twente Almelo Netherlands Not Yet Recruiting
Antoni van Leeuwenhoek Amsterdam Netherlands Not Yet Recruiting
Gelre ziekenhuis Apeldoorn Netherlands Not Yet Recruiting
Rijnstate ziekenhuis Arnhem Netherlands Not Yet Recruiting
Catharina Ziekenhuis Eindhoven Netherlands Recruiting
Universitait Medisch Centrum Groningen Groningen Netherlands Not Yet Recruiting
Zuyderland ziekenhuis Heerlen Netherlands Not Yet Recruiting
Medisch Centrum Leeuwarden Leeuwarden Netherlands Not Yet Recruiting
Leids Universitair Medisch Centrum Leiden Netherlands Not Yet Recruiting
Erasmus Medisch Centrum Rotterdam Netherlands Not Yet Recruiting
Elisabeth Tweesteden ziekenhuis Tilburg Netherlands Not Yet Recruiting
Universitair Medisch Centrum Utrecht Utrecht Netherlands Not Yet Recruiting
Oxford University Hospitals Oxford United Kingdom Not Yet Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05180864 on ClinicalTrials.gov ↗ ← All trials in Italy