L-Gastrectomy With the Intelligent Navigation 4K UHD 3D Endoscopic Imaging System
Primary Purpose
Stomach Neoplasms
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Laparoscopic gastrectomy with Intelligent Navigation 4K UHD 3D Endoscopic Imaging System
Sponsored by
About this trial
This is an interventional treatment trial for Stomach Neoplasms focused on measuring Laparoscopy, Gastrectomy, 4K, 3D, lymphadenectomy
Eligibility Criteria
Inclusion Criteria:
- Diagnosed with gastric cancer require surgery;
- Without a history of abdominal surgery;
- BMI ≤ 30 kg/m2;
- Preoperative ECOG score is 0~1 and ASA score is I~III;
- Having signed the Medical Informed Consent.
Exclusion Criteria:
- Patients with metastasis or invasion of surrounding tissues;
- Undergoing emergency operation (perforation, hemorrhage, obstruction);
- Patients with serious medical co-morbidity (heart, lung, liver and kidney diseases) and could not tolerate laparoscopic surgery;
- With poor incorrigible physical condition before surgery;
- The patient who underwent gastrojejunostomy or jejunostomy;
- The patient who refuses to accept standardized postoperative systemic therapy according to the guidelines.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
laparoscopic gastrectomy with Intelligent Navigation 4K UHD 3D
Arm Description
Outcomes
Primary Outcome Measures
The success rate of laparoscopic gastric surgery
Rate of successfully performed laparoscopic gastrectomy
Secondary Outcome Measures
Lymph node dissection rate
The numbers of lymph node dissected in the surgery
Full Information
NCT ID
NCT04526483
First Posted
August 19, 2020
Last Updated
August 21, 2020
Sponsor
Shanghai Minimally Invasive Surgery Center
1. Study Identification
Unique Protocol Identification Number
NCT04526483
Brief Title
L-Gastrectomy With the Intelligent Navigation 4K UHD 3D Endoscopic Imaging System
Official Title
Safety and Efficacy of a Novel Intelligent Navigation 4K UHD 3D Endoscopic Imaging System in Laparoscopic Gastrectomy
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 1, 2020 (Anticipated)
Primary Completion Date
October 1, 2022 (Anticipated)
Study Completion Date
October 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Minimally Invasive Surgery Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims to evaluate the safety, efficacy, and feasibility of the Intelligent Navigation 4K UHD 3D Endoscopic Imaging System in patients with gastric cancer.
Detailed Description
Background: Lymphadenectomy in laparoscopic gastrectomy can significantly improve the long-term survival and accuracy of the tumor staging of patients with gastric cancer. The retrieval of more lymph nodes has gradually become a trend among surgeons. However, lymphadenectomy is currently performed without the aid of visual instruments which might lead to an unknown pathological outcome and influence the prognosis of gastric cancer patients. And none of the indocyanine green (ICG) fluorescent imaging systems applied in clinical practice now is equipped with ultra-high definition (4K) or three-dimensional (3D) lens. To explore the advent of minimally invasive surgery with a conveniently switchable high-quality imaging system, we designed a new laparoscopic navigating technique that combined all the three characteristics.
Aims: This study aims to evaluate the safety, efficacy, and feasibility of the Intelligent Navigation 4K UHD 3D Endoscopic Imaging System in patients with gastric cancer.
Methods/design This is a prospective, one-arm, single-center, single-set target value clinical trial to investigate the clinical value of the Intelligent Navigation 4K UHD 3D Endoscopic Imaging System on laparoscopic gastric surgery. The trial will recruit a total of 67 participants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stomach Neoplasms
Keywords
Laparoscopy, Gastrectomy, 4K, 3D, lymphadenectomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
This is a prospective, one-arm, single-center, single-set target value clinical trial to investigate the clinical value of the Intelligent Navigation 4K UHD 3D Endoscopic Imaging System on laparoscopic gastric surgery. The trial will recruit a total of 67 participants.
Masking
None (Open Label)
Allocation
N/A
Enrollment
67 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
laparoscopic gastrectomy with Intelligent Navigation 4K UHD 3D
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Laparoscopic gastrectomy with Intelligent Navigation 4K UHD 3D Endoscopic Imaging System
Intervention Description
Laparoscopic gastrectomy with Intelligent Navigation 4K UHD 3D Endoscopic Imaging System
Primary Outcome Measure Information:
Title
The success rate of laparoscopic gastric surgery
Description
Rate of successfully performed laparoscopic gastrectomy
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Lymph node dissection rate
Description
The numbers of lymph node dissected in the surgery
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosed with gastric cancer require surgery;
Without a history of abdominal surgery;
BMI ≤ 30 kg/m2;
Preoperative ECOG score is 0~1 and ASA score is I~III;
Having signed the Medical Informed Consent.
Exclusion Criteria:
Patients with metastasis or invasion of surrounding tissues;
Undergoing emergency operation (perforation, hemorrhage, obstruction);
Patients with serious medical co-morbidity (heart, lung, liver and kidney diseases) and could not tolerate laparoscopic surgery;
With poor incorrigible physical condition before surgery;
The patient who underwent gastrojejunostomy or jejunostomy;
The patient who refuses to accept standardized postoperative systemic therapy according to the guidelines.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Junjun Ma
Phone
13917283686
Email
zmhtiger@yeah.net
First Name & Middle Initial & Last Name or Official Title & Degree
Minhua Zheng
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
L-Gastrectomy With the Intelligent Navigation 4K UHD 3D Endoscopic Imaging System
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