Randomized Controlled Trial on Effect of Lymph Node Mapping by Indocyanine Green Via Submucosal or Subserosal Injection

Sponsor
Fujian Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04219332
Collaborator
(none)
266
1
2
45.9
5.8

Study Details

Study Description

Brief Summary

The purpose of this study was to evaluate whether submucosal or subserous injection of indocyanine green during laparoscopic lymphadenectomy for patients with gastric cancer was different. The patients with gastric adenocarcinoma (cT1-4a, N0/+, M0) were studied.

Condition or Disease Intervention/Treatment Phase
  • Drug: Subserosa injection of indocyanine green
  • Drug: submucosal injection of indocyanine green
Phase 3

Detailed Description

In recent years, with the successful application of ICG (indocyanine green) fluorescence imaging technology in laparoscopic equipment, scholars have found that ICG near-infrared imaging has better tissue penetration and can better identify lymph nodes in hypertrophic adipose tissue than other dyes under visible light, which makes ICG fluorescence imaging guide laparoscopic radical resection of gastric cancer lymph node dissection has become a new exploration direction. ICG near-infrared imaging technology has important research value, good application prospects, and broad development space in laparoscopic radical resection of gastric cancer. However, at present, the application of ICG near-infrared imaging technology in laparoscopic radical resection of gastric cancer is still in the exploratory stage, and there is no unified standard. Therefore, in the world, there is still a lack of high-level evidence-based evidence of large-sample prospective randomized controlled trials to evaluate the effectiveness, safety, and feasibility of submucosal or subserous injection of ICG in guiding laparoscopic D2 resection of gastric cancer. The investigator first carried out this study in the world to evaluate the lymph node dissection and perioperative safety of gastric cancer patients who received a submucosal injection of ICG and subserous injection of ICG during laparoscopic radical gastrectomy in the same period, to promote the standardized development of ICG near-infrared imaging in laparoscopic radical gastrectomy.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
266 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison of Submucosal and Subserosal Approaches Toward Optimized Indocyanine Green Tracer-Guided Laparoscopic Lymphadenectomy for Patients With Gastric Cancer: The FUGES-019 Randomized Clinical Trial
Actual Study Start Date :
Dec 31, 2019
Actual Primary Completion Date :
Nov 27, 2020
Anticipated Study Completion Date :
Oct 28, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Subserosal injection of indocyanine green tracer group

Subserosal injection of indocyanine green, with a concentration of 0.5 mg /ml, 6 points along the lesser and greater curvature of the stomach, 1.5 ml for each point.

Drug: Subserosa injection of indocyanine green
After preoperative exploration, the indocyanine green powder (Dandong Yichuang Pharmaceutical Co) is dissolved in 0.5 mg/ml of sterile water and the prepared solution (1.5 ml for each point) is injected along the subserosal of the stomach at 6 specific points along the lesser and greater curvature of the stomach.
Other Names:
  • No other intervention
  • Active Comparator: Submucosal injection of indocyanine green tracer group

    Submucosal injection of indocyanine green, with a concentration of 1.25mg /ml, four points around the primary tumor, each point 0.5 ml.

    Drug: submucosal injection of indocyanine green
    One day before surgery, 1.25 mg/ml indocyanine green (Dandong Yichuang Pharmaceutical Co) was prepared in sterile water and 0.5 ml of the solution was injected into the submucosal layer at 4 quadrants around the primary tumor, amounting to 2.5 mg of indocyanine green.
    Other Names:
  • No other intervention
  • Outcome Measures

    Primary Outcome Measures

    1. Total Number of Retrieved Lymph Nodes [One month after surgery]

      Total Number of Retrieved Lymph Nodes

    Secondary Outcome Measures

    1. Total number of fluorescent lymph nodes in groups A and B [One month after surgery]

      Total number of fluorescent lymph nodes in groups A and B

    2. Relationship between fluorescent lymph nodes and positive lymph nodes in groups A and B (true positive rate) [One month after surgery]

      Relationship between fluorescent lymph nodes and positive lymph nodes in groups A and B (true positive rate)

    3. Relationship between fluorescent lymph nodes and negative lymph nodes in groups A and B (false positive rate) [One month after surgery]

      Relationship between fluorescent lymph nodes and negative lymph nodes in groups A and B (false positive rate)

    4. Relationship between non-fluorescent and negative lymph nodes in groups A and B (true negative rate) [One month after surgery]

      Relationship between non-fluorescent and negative lymph nodes in groups A and B (true negative rate)

    5. Relationship between non-fluorescent lymph nodes and positive lymph nodes in groups A and B (false negative rate) [One month after surgery]

      Relationship between non-fluorescent lymph nodes and positive lymph nodes in groups A and B (false negative rate)

    6. Number of Metastasis Lymph Nodes [One month after surgery]

      Number of Metastasis Lymph Nodes

    7. Metastasis rate of lymph node [One month after surgery]

      Metastasis rate of lymph node

    8. Mortality rates [30 days]

      This is for the early mortality, which defined as the event observed within 30 days after surgery.

    9. Morbidity rates [30 days]

      This is for the incidence of early postoperative complications, which defined as the event observed within 30 days after surgery.

    10. 3-year disease free survival rate [36 months]

      3-year disease free survival rate

    11. 3-year recurrence pattern [36 months]

      Recurrence patterns are classified into five categories at the time of first diagnosis: locoregional, hematogenous, peritoneal, distant lymph node, and mixed type.

    12. Time to first ambulation [30 days]

      Time to first ambulation in hours is used to assess the postoperative recovery course.

    13. Time to first flatus [30 days]

      Time to first flatus in days is used to assess the postoperative recovery course.

    14. Time to first liquid diet [30 days]

      Time to first liquid diet in days is used to assess the postoperative recovery course.

    15. Time to first soft diet [30 days]

      Time to first soft diet in days is used to assess the postoperative recovery course.

    16. Duration of postoperative hospital stay [30 days]

      Duration of postoperative hospital stay in days is used to assess the postoperative recovery course.

    17. The variation of weight [3, 6, 9 and 12 months]

      The variation of weight on postoperative 3, 6, 9 and 12 months are used to access the postoperative nutritional status and quality of life.

    18. The variation of BMI in kg/m^2 [3, 6, 9 and 12 months]

      The variation of BMI in kg/m^2 on postoperative 3, 6, 9 and 12 months are used to access the postoperative nutritional status and quality of life.

    19. Intraoperative morbidity rates [1 day]

      The intraoperative postoperative morbidity rates are defined as the rates of event observed within operation.

    20. The variation of white blood cell count [Preoperative 3 days and postoperative 1, 3, and 5 days]

      The 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.

    21. The variation of hemoglobin [Preoperative 3 days and postoperative 1, 3, and 5 days]

      The 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.

    22. The variation of C-reactive protein [Preoperative 3 days and postoperative 1, 3, and 5 days]

      The 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.

    23. Lymph node noncompliance rate [1 day]

      Lymph node noncompliance was defined as the absence of lymph nodes that should have been excised from more than 1 lymph node station. Major lymph node noncompliance was defined as more than 2 intended lymph node stations that were not removed.

    24. Modified EORTC cancer in-patient satisfaction with care measure (EORTC IN-PATSAT14) [30 days]

      Participants were asked to complete one modified European Organisation for Research and Treatment of Cancer (EORTC) IN-PATSAT14 questionnaire before their discharge from hospital.

    25. The Surgery Task Load Index (SURG-TLX) [1 day]

      Surgeons were required to complete one modified SURG-TLX questionnaire for each procedure.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion criteria:
    1. Age from 18 to 75 years

    2. Primary gastric adenocarcinoma (papillary, tubular, mucinous, signet ring cell, or poorly differentiated) confirmed pathologically by endoscopic biopsy

    3. Clinical stage tumor T1-4a (cT1-4a), N0/+, M0 at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual Eighth Edition. Preoperative staging was made by conducting mandatory computed tomography (CT) scans and an optional endoscopic ultrasound

    4. No distant metastasis, no direct invasion of pancreas, spleen or other organs nearby in the preoperative examinations

    5. Performance status of 0 or 1 on Eastern Cooperative Oncology Group scale (ECOG)

    6. American Society of Anesthesiology score (ASA) class I, II, or III

    7. Written informed consent

    Exclusion criteria:
    1. Women during pregnancy or breast-feeding

    2. Severe mental disorder

    3. History of previous upper abdominal surgery (except laparoscopic cholecystectomy)

    4. History of previous gastrectomy, endoscopic mucosal resection or endoscopic submucosal dissection

    5. Rejection of laparoscopic resection

    6. History of allergy to iodine agents

    7. Enlarged or bulky regional lymph node diameter over 3cm by preoperative imaging

    8. History of other malignant disease within past five years

    9. History of previous neoadjuvant chemotherapy or radiotherapy

    10. History of unstable angina or myocardial infarction within past six months

    11. History of cerebrovascular accident within past six months

    12. History of continuous systematic administration of corticosteroids within one month

    13. Requirement of simultaneous surgery for other disease

    14. Emergency surgery due to complication (bleeding, obstruction or perforation) caused by gastric cancer

    15. Forced expiratory volume in 1 second (FEV1)<50% of predicted values

    16. Linitis plastica, Widespread

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Gastric Surgery Fuzhou Fujian China

    Sponsors and Collaborators

    • Fujian Medical University

    Investigators

    • Study Chair: Chang-Ming Huang, MD, Fujian Medical University Union Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Chang-Ming Huang, Prof., Director, Head of Department of Gastric Surgery, Principal Investigator, Clinical Professor, Fujian Medical University
    ClinicalTrials.gov Identifier:
    NCT04219332
    Other Study ID Numbers:
    • FUGES-019
    First Posted:
    Jan 7, 2020
    Last Update Posted:
    Mar 24, 2021
    Last Verified:
    Mar 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 24, 2021