Sentinel Lymph Node Navigation Surgery Using Near-infrared Imaging in Early Esophageal Cancer
Primary Purpose
Detection Rate of SLN ; Accuracy Rate of Lymph Node Metastasis
Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Indocyanine Green for Injection
Sponsored by
About this trial
This is an interventional diagnostic trial for Detection Rate of SLN ; Accuracy Rate of Lymph Node Metastasis
Eligibility Criteria
Inclusion Criteria:
- 18 years old ≤ age ≤ 75 years old, gender is not limited;
- patient who is diagnosed with ESCC and choose to proceed with surgery
- patient with cTNM stage:T1-3N0-1M0
- tumor located at the middle thoracic or lower thoracic esophagus
- The main organ function is basically normal: Karnofsky score >70%;
- Laboratory blood tests meet surgical standards;
Exclusion Criteria:
- pregnancy or breastfeeding
- history of iodide or seafood allergy,
- Patient with occult metastatic disease at the time of surgery
- patient with mental disorder;
- Patient who is simultaneously involved in another clinical trial;
Sites / Locations
- The Fifth Affiliated Hospital of Sun Yat-sen UniversityRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
use of indocyanine green
Arm Description
submucosal injection of ICG is by gastroscopy on the superior and inferior edge of the esophageal tumor,Dose of 0.5mg
Outcomes
Primary Outcome Measures
the detection rate of sentinel lymph node
the detection rate of sentinel lymph node in all the enrolled patients
The positive rate of sentinel lymph node
the positive rate of sentinel lymph node in all the enrolled patients
Secondary Outcome Measures
Full Information
NCT ID
NCT04173676
First Posted
November 17, 2019
Last Updated
February 22, 2021
Sponsor
Fifth Affiliated Hospital, Sun Yat-Sen University
Collaborators
Sun Yat-sen University
1. Study Identification
Unique Protocol Identification Number
NCT04173676
Brief Title
Sentinel Lymph Node Navigation Surgery Using Near-infrared Imaging in Early Esophageal Cancer
Official Title
Sentinel Lymph Node Navigation Using Near-infrared Imaging in Radical Esophagectomy Surgery :a Single-arm Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 2, 2019 (Actual)
Primary Completion Date
November 30, 2021 (Anticipated)
Study Completion Date
November 30, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fifth Affiliated Hospital, Sun Yat-Sen University
Collaborators
Sun Yat-sen University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The esophageal squamous cell carcinoma (ESCC) has high prevalence and mortality in China, which become a severe challenge for public health. Esophagectomy is the preferred choice for the patients who are diagnosed with ESCC in early stage .Although three-field lymphadenectomy has improved patient survival and reduced tumor recurrence, Surgery-related complications increased dramatically.
It has become a research hotspot to find an effective detection method to identify the lymph node metastasis of ESCC and avoid ineffective expanded lymphadenectomy .The molecular imaging technology has been developed for intra-operative visualization and precise resection of the tumors.
Indocyanine Green for Injection (ICG) has been used as a contrast agent in the near-infrared imaging system for the surgical navigation technology, which has a relatively positive effect in the clinical application of gastric cancer and liver cancer.There are few reports on the application of ICG near-infrared imaging tracer lymph nodes in the surgery of ESCC. This study intends to identify the detection rate of sentinel lymph node (SLN) and determine the accuracy of regional lymph node metastasis in ESCC by ICG near-infrared imaging technique, which provides clinical evidence for subsequent precise resection of the lymph nodes.
This will be one-arm prospective trial. The ESCC patients will be recruited with strict criteria. 84 patients will be enrolled between18 and 75 years old, without gender limit. The submucosal injection of ICG will be performed preoperatively by gastroscopy on the superior and inferior edge of the esophageal tumor. NIR fluorescence imaging will be performed intraoperatively to observe the lymph nodes. The luminescent lymph node is defined as SLN. According to the standard procedure, 3 field lymphadenectomy will be performed, and all the resected lymph nodes will be subjected to pathological analysis including correlation study of fluorescence signal and tumor tissue in pathology slice.
This clinical trial is anticipated to evaluate the detection rate of SLN in ESCC with ICG near-infrared fluorescence imaging and determine the accuracy of regional lymph node metastasis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Detection Rate of SLN ; Accuracy Rate of Lymph Node Metastasis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Model Description
The sentinel lymph nodes are observed by submucosal injection of ICG
Masking
None (Open Label)
Allocation
N/A
Enrollment
84 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
use of indocyanine green
Arm Type
Experimental
Arm Description
submucosal injection of ICG is by gastroscopy on the superior and inferior edge of the esophageal tumor,Dose of 0.5mg
Intervention Type
Drug
Intervention Name(s)
Indocyanine Green for Injection
Intervention Description
The sentinel lymph nodes were observed by submucosal injection of ICG
Primary Outcome Measure Information:
Title
the detection rate of sentinel lymph node
Description
the detection rate of sentinel lymph node in all the enrolled patients
Time Frame
through study completion, an average of 1 year
Title
The positive rate of sentinel lymph node
Description
the positive rate of sentinel lymph node in all the enrolled patients
Time Frame
through study completion, an average of 1 year
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:
18 years old ≤ age ≤ 75 years old, gender is not limited;
patient who is diagnosed with ESCC and choose to proceed with surgery
patient with cTNM stage:T1-3N0-1M0
tumor located at the middle thoracic or lower thoracic esophagus
The main organ function is basically normal: Karnofsky score >70%;
Laboratory blood tests meet surgical standards;
Exclusion Criteria:
pregnancy or breastfeeding
history of iodide or seafood allergy,
Patient with occult metastatic disease at the time of surgery
patient with mental disorder;
Patient who is simultaneously involved in another clinical trial;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hong Shan, PhD
Phone
+86-18826913336
Email
shanhong@mail.sysu.edu.cn
Facility Information:
Facility Name
The Fifth Affiliated Hospital of Sun Yat-sen University
City
Zhuhai
State/Province
Guangdong
ZIP/Postal Code
519000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaojin Wang, MD
Phone
+86-13798967219
Email
wangxj55@mail.sysu.edu.cn
12. IPD Sharing Statement
Plan to Share IPD
No
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Sentinel Lymph Node Navigation Surgery Using Near-infrared Imaging in Early Esophageal Cancer
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