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Indocyanine Green Tracer Using in Laparoscopic Gastrectomy With Lymph Node Dissection

Prospective Randomized Controlled Trials on Clinical Outcomes of Indocyanine Green Tracer Using in Laparoscopic Gastrectomy With Lymph Node Dissection for Gastric Cancer

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03050879
Acronym
ICGTinLG
Enrollment
266
Registered
2017-02-13
Start date
2017-10-15
Completion date
2019-07-13
Last updated
2025-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Indocyanine Green, Stomach Neoplasms

Keywords

Stomach Neoplasms, Indocyanine Green Tracer, Laparoscopic Gastrectomy, Lymph Node Dissection

Brief summary

The purpose of this study is to explore the clinical outcomes of Indocyanine Green Tracer using in laparoscopic gastrectomy with lymph node dissection for gastric adenocarcinoma(cT1-4a, N-/+, M0).

Detailed description

Indocyanine Green Tracer is often applied in surgery for early gastric adenocarcinoma. Its application in laparoscopic gastrectomy with lymph node dissection for gastric adenocarcinoma is at the stage of cases accumulation, method studying and clinical research. There is no prospective studies to identify the clinical outcomes of Indocyanine Green Tracer using in laparoscopic gastrectomy with lymph node dissection for gastric adenocarcinoma. On the basis of more than 3000 cases of laparoscopic gastrectomy with lymph node dissection for gastric adenocarcinoma, we want to apply the Indocyanine Green Tracer, a cheap, easy to operate and no radiation pollution way, to predict the positive lymph nodes in gastric adenocarcinoma, to guid the scope of laparoscopic lymph node dissection for gastric adenocarcinoma.

Interventions

Laparoscopic gastrectomy with lymph node dissection for gastric cancer using Indocyanine Green Tracer

Sponsors

Fujian Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age from 18 to 75 years * Primary gastric adenocarcinoma (papillary, tubular, mucinous, signet ring cell, or poorly differentiated) confirmed pathologically by endoscopic biopsy * clinical stage tumor 1-4a (cT1-4a), N-/+, M0 at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual Seventh Edition * No distant metastasis, no direct invasion of pancreas, spleen or other organs nearby in the preoperative examinations * Performance status of 0 or 1 on Eastern Cooperative Oncology Group scale (ECOG) * American Society of Anesthesiology score (ASA) class I, II, or III * Written informed consent

Exclusion criteria

* Women during pregnancy or breast-feeding * Severe mental disorder * History of previous upper abdominal surgery (except laparoscopic cholecystectomy) * History of previous gastrectomy, endoscopic mucosal resection or endoscopic submucosal dissection * Enlarged or bulky regional lymph node diameter over 3cm by preoperative imaging * History of other malignant disease within past five years * History of previous neoadjuvant chemotherapy or radiotherapy * History of unstable angina or myocardial infarction within past six months * History of cerebrovascular accident within past six months * History of continuous systematic administration of corticosteroids within one month * Requirement of simultaneous surgery for other disease * Emergency surgery due to complication (bleeding, obstruction or perforation) caused by gastric cancer * FEV1\<50% of predicted values * Diffuse; widespread; plastica

Design outcomes

Primary

MeasureTime frameDescription
Total Number of Retrieved Lymph Nodes14 daysCompare total number of retrieved lymph nodes in both group.

Secondary

MeasureTime frameDescription
Positive rate14 daysThe number of positive lymph nodes in fluorescent lymph nodes is divided by the number of total fluorescent lymph nodes in experimental group
False positive rate14 daysThe number of negative lymph nodes in fluorescent lymph nodes is divided by the number of total fluorescent lymph nodes in experimental group
Negative rate14 daysThe number of negative lymph nodes in not fluorescent lymph nodes is divided by the number of total not fluorescent lymph nodes in experimental group
False negative rate14 daysThe number of positive lymph nodes in not fluorescent lymph nodes is divided by the number of total not fluorescent lymph nodes in experimental group
Number of Metastasis Lymph Nodes14 daysCompare number of positive lymph nodes in both group.
Metastasis rate of lymph node14 daysCompare metastasis rate of lymph node in both group
Morbidity and mortality rates30 daysThis is for the early postoperative complication and mortality, which defined as the event observed within 30 days after surgery.
3-year disease free survival rate36 monthsdisease-free survival was defined as the time from surgery to the time of recurrence or death from any cause
3-year recurrence pattern36 monthsRecurrence patterns are classified into five categories at the time of first diagnosis: locoregional, hematogenous, peritoneal, distant lymph node, and mixed type.
Postoperative recovery course10 daysTime to first ambulation, flatus, liquid diet and soft diet, duration of postoperative hospital stay and postoperative pain are used to assess the postoperative recovery course.Visual analog pain score method is used to evaluate the difference of postoperative pain degree.
Operation time1 day
The variation of weight3, 6, 9 and 12 monthsThe variation of weight on postoperative 3, 6, 9 and 12 months are used to access the postoperative nutritional status and quality of life.
Intraoperative blood loss1 day
Conversive rate1 day
The rate of fluorescence14 daysThe number of fluorescent lymph node in experimental group is divided by the total number of lymph nodes in active experimental group
Incision length1 day
The variation of cholesterol3, 6, 9 and 12 monthsThe variation of cholesterol in millimole/liter on postoperative 3, 6, 9 and 12 months are used to access the postoperative nutritional status and quality of life.
The variation of album3, 6, 9 and 12 monthsThe variation of album in gram/liter on postoperative 3, 6, 9 and 12 months are used to access the postoperative nutritional status and quality of life.
The results of endoscopy3, 6, 9 and 12 monthsThe incidence of reflux esophagitis under the endoscopy on postoperative 3 and 12 months are used to access the postoperative quality of life.
The variation of body temperature8 daysThe daily highest body temperature in degree centigrade before discharge are recorded to access the inflammatory and immune response.
The variation of white blood cell countPreoperative 3 days and postoperative 1, 3, and 5 daysThe values of white blood cell count from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory and immune response.
The variation of hemoglobinPreoperative 3 days and postoperative 1, 3, and 5 daysThe values of hemoglobin in gram/liter from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory and immune response.
The variation of C-reactive proteinPreoperative 3 days and postoperative 1, 3, and 5 daysThe values of C-reactive protein IN milligram/liter from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory and immune response.
The variation of prealbuminPreoperative 3 days and postoperative 1, 3, and 5 daysThe values of prealbumin in gram/liter from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory and immune response.
3-year overall survival rate36 monthsOverall survival was defined as the time from surgery to death from any cause
5-year overall survival rate60 monthsOverall survival was defined as the time from surgery to death from any cause
5-year disease free survival rate60 monthsdisease-free survival was defined as the time from surgery to the time of recurrence or death from any cause
5-year recurrence pattern60 monthsRecurrence patterns are classified into five categories at the time of first diagnosis: locoregional, hematogenous, peritoneal, distant lymph node, and mixed type.
Intraoperative morbidity rates1 dayThe intraoperative postoperative morbidity rates are defined as the rates of event observed within operation.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026