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Trial Title:
Comparison Partial Versus Total Omentectomy in Minimal Invasive Distal Gastrectomy for cT3/4a Gastric Cancer (KLASS-10)
NCT ID:
NCT06608381
Condition:
Gastric Cancer
Conditions: Official terms:
Stomach Neoplasms
Study type:
Interventional
Study phase:
Phase 3
Overall status:
Recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Intervention model description:
Random group assignment during operation
- Control group : Total omentectomy
- Experimental group : Partial omentectomy Other surgical procedures are the same as
usual in both groups.
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Procedure
Intervention name:
Arm I (Total omentectomy),
Description:
The surgery is performed with minimal invasive surgery, and the range of the surgery is
radical gastrectomy and D2 lymph node dissection. Depending on the random assignment,
total omentectomy and partial omentectomy (omentum preservation) will be performed for
the control group and the experimental group, respectively. Total omentectomy removes
whole greater omentum, while partial omentectomy preserves the omentum more than 3cm away
from the gastro-epiploic vessels. Other surgical procedures are the same as usual in both
groups.
Arm group label:
Total omentectomy group
Intervention type:
Procedure
Intervention name:
Arm II (Partial omentectomy)
Description:
The surgery is performed with minimal invasive surgery, and the range of the surgery is
radical gastrectomy and D2 lymph node dissection. Depending on the random assignment,
total omentectomy and partial omentectomy (omentum preservation) will be performed for
the control group and the experimental group, respectively. Total omentectomy removes
whole greater omentum, while partial omentectomy preserves the omentum more than 3cm away
from the gastro-epiploic vessels. Other surgical procedures are the same as usual in both
groups.
Arm group label:
Partial omentectomy group
Summary:
For advanced gastric cancer, surgical resection is the only curable therapeutic strategy.
According to minimally invasive approach is adopted in various field of oncologic
surgery, laparoscopic gastrectomy with lymph node dissection is becoming a standard not
only for early gastric cancer but also for advanced gastric cancer.
The greater omentum is an organ is known to play a role in removing bacteria in the
abdominal cavity as a primary defense. Complete resection of the greater omentum has been
considered essential to ensure the elimination of micrometastasis during surgery for
advanced gastric cancer. However, the oncological effect of total omentectomy is still
lack of evidence. Especially in minimal invasive gastrectomy, total omentectomy procedure
is known to increases the operating time, increase the risk of bleeding, colonic injury,
and postoperative complications such as intra-abdominal abscess, ascites, anastomotic
leakage, ileus and wound infections. Therefore, in the case of minimal invasive surgery
in early gastric cancer, omentectomy is omitted usually or routinely. Partial omentectomy
preserves the omentum more than 3cm away from the gastro-epiploic vessels. Advanced
energy devices facilitate partial omentectomy during laparoscopic gastrectomy.
According to the Japanese Gastric Cancer Treatment Guidelines, partial omentectomy
(omentum preservation) is feasible for T1 or T2 tumors, and total omentectomy is
recommended for clinical T3 or deeper tumors. However, the National Comprehensive Cancer
Network(NCCN) guideline suggests total omentectomy and the European Society for Medical
Oncology(ESMO) guideline does not mentioned about it.
It is still controversial whether total omentectomy should be performed in advanced
gastric cancer. Therefore, we aimed to verify the non-inferiority of partial omentectomy,
oncologic safety compared with total omentectomy via multicenter randomized clinical
trial.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Histologically proven adenocarcinoma of the stomach
- Age between 20 to 85 years old
- ECOG PS 0-1, ASA class I-III
- Endoscopically Borrmann type I, II, III
- Clinical T3 and T4a tumors with or without regional lymph node metastases
(cT3N0M0~T4aN3M0)
- Capable of minimal invasive radical subtotal gastrectomy with R0 resection in
preoperative examinations
- Patients who signed an written consent form approved by the Institutional Review
Board(IRB) after receiving sufficient explanations of the contents of the clinical
trial
- Domestic patients who are able to follow up for 3 years after surgery
Exclusion Criteria:
- Confirmed distant metastasis in preoperative examinations
- Confirmed metastasis in abdominal cavity or distant organs during surgery
- Confirmed no infiltration of the serosa layer or unable to confirm the tumor
location during surgery (sT1-2)
- Confirmed invasion of surrounding organs (sT4b)
- History of previous gastrectomy or greater omentum related surgery
- Patients who underwent preoperative treatment (chemotherapy, radiotherapy, or
endoscopic submucosal dissection) for recently diagnosed gastric cancer
- Synchronous or metachronous malignancies, which underwent surgery, chemotherapy or
radiotherapy within 5 years
- Patients judged to be inappropriate for the study by the physician. (ex. Pregnancy)
- Patients refused to participate after random assignment
- Surgery is not performed until 30 days after consenting to participate
- Patients who has participated in another on-going clinical trial, which is related
surgical procedures and survival.
Gender:
All
Minimum age:
20 Years
Maximum age:
85 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
GangnamSeverance Hospital
Address:
City:
Seoul
Country:
Korea, Republic of
Status:
Recruiting
Contact:
Last name:
Jieun Jung
Phone:
82-2-2019-4601
Email:
gsirb@yuhs.ac
Start date:
June 26, 2024
Completion date:
December 30, 2031
Lead sponsor:
Agency:
Gangnam Severance Hospital
Agency class:
Other
Source:
Gangnam Severance Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06608381