Feasibility and Safety of Robotic Assisted Proximal Gastrectomy With Double-flap Technique for Proximal Early Gastric Cancer

Feasibility and Safety of Robotic Assisted Proximal Gastrectomy With Double-flap Technique for Proximal Early Gastric Cancer: a Phase II, Multi-center, Single-arm Clinical Study

Proximal early gastric cancer can choose radical total gastrectomy or proximal gastrectomy. The patients have poor nutritional status and quality of life after total gastrectomy. Compare to total gastrectomy, the nutritional status can improve after proximal gastrectomy . But if use simple esophagogastric anastomosis for proximal gastrectomy, the incidence of postoperative reflux esophagitis is high, which seriously affects the quality of life, and the short-term outcome is poorer than the total gastrectomy. If the incidence of postoperative reflux esophagitis can be reduced, proximal gastrectomy would be the treatment choice for proximal early gastric cancer, which may more improve both quality of life and nutritional condition than total gastrectomy.

Double-flap technique is a new surgical reconstruction procedure between esophagus and remnant stomach. It can reduce the occurrence of reflux oesophagitis through reconstruction a simulative cardia. At present, the technique has been carried out in some hospitals in China but still lack large-scale prospective studies and evidence of evidence-based medicine. At present, some retrospective studies have shown that robotic assisted proximal gastrectomy with double-flap technique is safe and effective, and the learning curve is shorter than laparoscopic surgery. The applicant have finished two robotic assisted proximal gastrectomy with double-flap technique cases. Two patients recovered well after surgery, with no occurrence of anastomotic leakage or stenosis and the postoperative quality of life was good. Now we plan to conduct a multi-center, single arm study on proximal early gastric cancer patients(T1N0-1M0 and T2N0M0) to evaluate the feasibility of robotic assisted proximal gastrectomy with double-flap technique , and to evaluate the surgical and oncological safety of this surgical method. Aim to provide initial evidence of evidence-based medicine for its clinical application..

Study Overview

Status

Not yet recruiting

Conditions

Study Type

Interventional

Enrollment (Estimated)

42

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 Contact

  • Name: Yang bin, associate professor
  • Phone Number: 13798163278
  • Email: yyzsu@163.com

Study Locations

    • Guangdong
      • Guangzhou, Guangdong, China
        • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
        • Contact:

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. 20 years ≤ age ≤ 80 years
  2. The primary gastric lesions were located in the proximal third of the stomach
  3. histologically proven gastric adenocarcinoma (by preoperative gastrofiberscopy)
  4. clinical stage IA (T1N0M0) or IB (T1N1M0 / T2N0M0) according to the 8th edition of the American Joint Committee on Cancer System(Clinical stage was determined based on the finding of endoscopic ultrasonography and/or thoraco-abdominal contrast-enhanced computed tomography)
  5. scheduled for robotic assisted proximal gastrectomy with D1+/D2 lymphadenectomy, and possible for R0 surgery by this procedures (Lymphadenectomy is performed on the basis of the criteria of the Japanese Gastric Cancer Treatment Guidelines 2021 (6th edition).).
  6. The preoperative American Society of Anesthesiologists (ASA) physical status was I-III;
  7. The patient's cardiopulmonary function can tolerate robotic assisted surgery;
  8. The subjects have signed the informed consent form.

Exclusion Criteria:

  1. history of upper abdominal surgery and not suitable for robotic assisted surgery
  2. the tumor invades the esophagus 3cm above gastro-esophageal junction (Z-line)
  3. with other malignant diseases or have suffered from other malignant diseases within 5 years
  4. Excessive tension for esophagogastric anastomosis and require changing the reconstruction procedure
  5. women are pregnant or in lactation period
  6. Suffering from serious mental illness
  7. history of continuous systemic corticosteroid or immunosuppressive drug treatment within 1 month

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Robotic assisted proximal gastrectomy with double-flap technique
Patients in this group receive robotic assisted proximal gastrectomy with D1+/D2 lymph node dissection(D1+ for stage IA:Nos.1, 2, 3a, 4 sa, 4 sb, 7, 8a, 9,11p;D2 for stage IB: Nos.1, 2, 3a, 4 sa, 4 sb, 7, 8a, 9,11p and 11d).The double-flap technique is used for the digestive tract reconstruction.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Proportion of Patients With Reflux Esophagitis Within 12 Months Postoperatively
Time Frame: 12 months postoperatively
During follow-up endoscopy 1 year after surgery, reflux esophagitis were graded according to the Los Angeles (LA) classification.
12 months postoperatively

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality of Life after Surgery
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively
Quality of life(QoL) is evaluated using the European Organization for Research and Treatment of Cancer (EORTC) 30-item core QoL (QLQ-C30 ver.3.0). Higher scores mean a worse outcome.
Follow-up evaluations are performed 3, 6 and 12 months postoperatively
Gastrointestinal Symptoms after Surgery
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively
gastrointestinal symptoms are assessed by Gastrointestinal Quality of Life Index (GIQLI) questionnaires. Higher scores mean a better outcome.
Follow-up evaluations are performed 3, 6 and 12 months postoperatively
Late Postoperative Morbidity
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
adhesive ileus, anastomosis stenosis, malnutrition, dumping syndrome. All postoperative complications are classified according to the Clavien-Dindo(CD) classification standard.
Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
Early Postoperative Morbidity
Time Frame: From surgery to discharge, up to 30 days
operation wound with seroma, hematoma, infection, dehiscence, or evisceration, anastomotic leakage, anastomotic bleeding, abdominal bleeding, abdominal abscess, intestinal obstruction morbidity, gastrointestinal bleeding, gastroparesis, postoperative pancreatitis, pancreatic fistula, chylous leakage, lung morbidity, cerebrovascular morbidity, cardiovascular morbidity, deep vein thrombosis, cholecystitis, liver dysfunction, kidney dysfunction. All postoperative complications are classified according to the Clavien-Dindo(CD) classification standard.
From surgery to discharge, up to 30 days
Short-term Clinical Outcome After Surgery
Time Frame: From surgery to discharge, up to 30 days
time to pass gas(hours)
From surgery to discharge, up to 30 days
Short-term Clinical Outcome After Surgery
Time Frame: From surgery to discharge, up to 30 days
time to oral intake(hours)
From surgery to discharge, up to 30 days
Short-term Clinical Outcome After Surgery
Time Frame: From surgery to discharge, up to 30 days
time to indwell gastric tube(hours)
From surgery to discharge, up to 30 days
Short-term Clinical Outcome After Surgery
Time Frame: From surgery to discharge, up to 30 days
length of postoperative hospitalisation(days)
From surgery to discharge, up to 30 days
Surgical Characteristics
Time Frame: 24 hours postoperatively
operative time(minutes)
24 hours postoperatively
Surgical Characteristics
Time Frame: 24 hours postoperatively
time for reconstruction the digestive tract(minutes) during surgery
24 hours postoperatively
body mass index postoperatively
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
body mass index(kg/m^2)
Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
Quality of Life postoperatively
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively
Quality of life(QoL) is evaluated using the European Organization for Research and Treatment of Cancer (EORTC) gastric cancer module (QLQ-STO22) questionnaire. Higher scores mean a worse outcome.
Follow-up evaluations are performed 3, 6 and 12 months postoperatively
Pathological Characteristics
Time Frame: 1 week postoperatively
lymph nodes dissection extent for each patient in the surgery
1 week postoperatively
Pathological Characteristics
Time Frame: 1 week postoperatively
number of dissected lymph nodes for each patient in the surgery
1 week postoperatively
Pathological Characteristics
Time Frame: 1 week postoperatively
R0 resection rate. R0 resection represents complete resection of the tumor, meaning there is no residual tumor.
1 week postoperatively
Proportion of participants die after surgery
Time Frame: From surgery to discharge, up to 30 days
mortality rate
From surgery to discharge, up to 30 days
Changes in total protein at Follow-up
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
blood total protein(g/L) levels
Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
Changes in serum albumin at Follow-up
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
blood serum albumin(g/L) levels
Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
Changes in prealbumin at Follow-up
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
blood prealbumin(g/L) levels
Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
Changes in hemoglobin at Follow-up
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
blood hemoglobin(g/L) levels
Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
Changes in Vitamin B12 at Follow-up
Time Frame: Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
blood Vitamin B12(μg/ml) levels
Follow-up evaluations are performed 3, 6 and 12 months postoperatively.
Surgical Characteristics
Time Frame: 24 hours postoperatively
blood loss during surgery(ml)
24 hours postoperatively
pain assessment postoperatively
Time Frame: Day 1 postoperatively
We measured the pain score using visual analog scale(VAS) at 24 h after the surgery is completed. Higher scores mean a worse outcome.
Day 1 postoperatively
Proportion of participants need to rehospitalized after surgery
Time Frame: From surgery to discharge, up to 30 days
rehospitalization rate
From surgery to discharge, up to 30 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Estimated)

June 10, 2023

Primary Completion (Estimated)

December 10, 2026

Study Completion (Estimated)

December 10, 2026

Study Registration Dates

First Submitted

May 4, 2023

First Submitted That Met QC Criteria

May 28, 2023

First Posted (Actual)

June 7, 2023

Study Record Updates

Last Update Posted (Actual)

June 7, 2023

Last Update Submitted That Met QC Criteria

May 28, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

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.

Clinical Trials on Stomach Neoplasms

Clinical Trials on Robotic assisted proximal gastrectomy with double-flap technique

3
Subscribe