Clinical Outcomes of Indocyanine Green Tracer Using in Laparoscopic Gastrectomy With Lymph Node Dissection for Remnant Gastric Cancer

Sponsor
Fujian Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05618821
Collaborator
(none)
68
1
2
69.9
1

Study Details

Study Description

Brief Summary

Patients with resectable remnant gastric cancer were selected as study subjects to investigate the safety, efficacy, and feasibility of ICG near-infrared imaging tracing in guiding laparoscopic lymph node dissection for remnant gastric cancer by comparing injection ICG group and non-injection ICG group.

Condition or Disease Intervention/Treatment Phase
  • Drug: Indocyanine Green Tracer
Phase 2

Detailed Description

Indocyanine Green Tracer is often applied in surgery for gastric cancer. Its application in laparoscopic gastrectomy with lymph node dissection for remnant gastric cancer 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 remnant gastric cancer. On the basis of more than 300 cases of laparoscopic gastrectomy with lymph node dissection for remnant gastric cancer, 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 remnant gastric cancer, to guid the scope of laparoscopic lymph node dissection for remnant gastric cancer.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
68 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Clinical Outcomes of Indocyanine Green Tracer Using in Laparoscopic Gastrectomy With Lymph Node Dissection for Remnant Gastric Cancer
Actual Study Start Date :
Jun 3, 2022
Anticipated Primary Completion Date :
Apr 1, 2025
Anticipated Study Completion Date :
Apr 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: ICG

Laparoscopic gastrectomy Group with the use of near-infrared imaging (ICG group)

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

Active Comparator: Non-ICG

Laparoscopic gastrectomy Group without the use of near-infrared imaging (Non-ICG group)

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

Outcome Measures

Primary Outcome Measures

  1. Total Number of Retrieved Lymph Nodes [30 days]

    Total Number of Retrieved Lymph Nodes

Secondary Outcome Measures

  1. Lymph node noncompliance rate [30 days]

    Lymph node noncompliance rate

  2. Relationship between fluorescent lymph nodes in the ICG group and total number of lymph nodes in the ICG group [30 days]

    Relationship between fluorescent lymph nodes in the ICG group and total number of lymph nodes in the ICG group

  3. Relationship between fluorescent lymph nodes in the ICG group and positive lymph nodes in the ICG group (positive rate) [30 days]

    Relationship between fluorescent lymph nodes in the ICG group and positive lymph nodes in the ICG group (positive rate)

  4. Relationship between fluorescent lymph nodes in the ICG group and negative lymph nodes in the ICG group (false positive rate) [30 days]

    Relationship between fluorescent lymph nodes in the ICG group and negative lymph nodes in the ICG group (false positive rate)

  5. Relationship between non-fluorescent lymph nodes in the ICG group and negative lymph nodes in the ICG group (negative rate) [30 days]

    Relationship between non-fluorescent lymph nodes in the ICG group and negative lymph nodes in the ICG group (negative rate)

  6. Number of Metastasis Lymph Nodes [30 days]

    Number of Metastasis Lymph Nodes

  7. Metastasis rate of lymph node [30 days]

    Metastasis rate of lymph node

  8. Postoperative morbidity rate [30 days]

    Postoperative morbidity rate

  9. Postoperative mortality rate [30 days]

    Postoperative mortality rate

  10. 3-year overall survival rate [3 years]

    3-year overall survival rate

  11. 3-year disease-free survival rate [3 years]

    3-year disease-free survival rate

  12. 3-year recurrence pattern [3 years]

    3-year recurrence pattern

  13. Postoperative recovery course [30 days]

    Time to first ambulation, flatus, liquid diet and soft diet, and postoperative hospital stay

  14. Intraoperative situation [30 days]

    Operation time, intraoperative blood loss, and intraoperative morbidity rate

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. Remnant gastric cancer (cT1-4a, N-/+, M0 at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual Seventh Edition)

(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 the ECOG (Eastern Cooperative Oncology Group) scale (6) ASA (American Society of Anesthesiology) class I to 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 for laparoscopic cholecystectomy and gastrectomy)

  4. History of previous gastric surgery (including ESD/EMR for gastric cancer)

  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 the past six months

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

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

  13. Requirement of simultaneous surgery for another disease

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

  15. FEV1<50% of the predicted values

  16. Linitis plastica, Widespread

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fujian Medical University Union Hospital Fuzhou Fujian China 350000

Sponsors and Collaborators

  • Fujian Medical University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Chang-Ming Huang, Prof., Professor, Fujian Medical University
ClinicalTrials.gov Identifier:
NCT05618821
Other Study ID Numbers:
  • FUGES-027
First Posted:
Nov 16, 2022
Last Update Posted:
Nov 16, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Chang-Ming Huang, Prof., Professor, Fujian Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 16, 2022