- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05360069
Linear Stapler Versus Circular Stapler in Esophagojejunostomy
March 29, 2026 updated by: Yunhong Tian, Nanchong Central Hospital
Linear Stapler Versus Circular Stapler in Esophagojejunostomy for Patients With Gastric Cancer Underwent Laparoscopic Total Gastrectomy
With the development of stapler devices, various methods of esophagojejunostomy after laparoscopic total gastrectomy were evoluated.
Which stapler is more advantageous has not been determined.
At present, the most commonly used is linear stapler or Circular stapler in esophagojejunostomy.
However, there is still a lack of reliable evidence for the selection of the two staplers.
The purpose of this study is to explore the advantages of linear staper versus circular stapler in esophagojejunostomy for patients with gastric cancer who underwent total gastrectomy.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
With the development of stapler devices, various methods of esophagojejunostomy after laparoscopic total gastrectomy were evoluated.
Which stapler is more advantageous has not been determined.
At present, the most commonly used is linear stapler or Circular stapler in esophagojejunostomy.
However, there is still a lack of reliable evidence for the selection of the two staplers.
The purpose of this study is to explore the advantages of linear staper versus circular stapler in esophagojejunostomy for patients with Siewert classification type II and III gastric cancer who underwent total gastrectomy.
Study Type
Interventional
Enrollment (Estimated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Sichuan
-
Nanchong, Sichuan, China, 637000
- Recruiting
- Yunhong Tian
-
Contact:
- Yunhong Tian, Doctor
- Phone Number: +8613508087719
- Email: drtianyunhong@126.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Histologically confirmed adenocarcinoma of the stomach, T1-T4 stages.
- Eastern Cooperative Oncology Group performance status of 0 or 1.
- Adequate organ function.
Exclusion Criteria:
- Patients had distant metastasis.
- oesophageal invasion of more than 3 cm.
- Borrmann type 4 or large (more than 8 cm) type 3 carcinoma.
- Previous chemotherapy or radiation therapy for any other malignancies.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Linear stapler group
Linear stapler is adopted in esophagojejunostomy.
|
Linear stapler is adopted in esophagojejunostomy
|
|
Active Comparator: Circular stapler group
Circular stapler is adopted in esophagojejunostomy.
|
Circular stapler is adopted in esophagojejunostomy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Surgical complication
Time Frame: 6 months
|
All surgical complication after laparoscopic total gastrectomy
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Operation duration
Time Frame: 1 day
|
operation time
|
1 day
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
hospitalization cost
Time Frame: 2 months
|
the cost in hospitalization
|
2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2020
Primary Completion (Estimated)
December 31, 2028
Study Completion (Estimated)
December 31, 2028
Study Registration Dates
First Submitted
March 11, 2022
First Submitted That Met QC Criteria
May 2, 2022
First Posted (Actual)
May 4, 2022
Study Record Updates
Last Update Posted (Actual)
April 2, 2026
Last Update Submitted That Met QC Criteria
March 29, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202101
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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