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Application of Indocyanine Green Labeled Fluorescent Laparoscopy in Proximal Gastric Cancer

Primary Purpose

Gastric Cancer

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
indocyanine green labeled fluorescent laparoscopy
Sponsored by
Guangyong Zhang
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Cancer focused on measuring Indocyanine green

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 18 years old < age < 75 years old
  2. The primary gastric lesion was pathologically diagnosed as proximal gastric adenocarcinoma by endoscopic biopsy (papillary adenocarcinoma PAP, tubular adenocarcinoma TUB, mucinous adenocarcinoma MUC, signed-ring cell carcinoma SIG, poorly differentiated adenocarcinoma POR)
  3. Preoperative clinical staging was CT1-4A, N-/+, and M0, according to AJCC-8th TNM tumor staging
  4. No distant metastasis was found in preoperative examination, and the tumor did not directly invade pancreas, spleen or other adjacent organs
  5. ECOG physical status score 0/1 before surgery Preoperative ASA score I-III

(7) Informed consent of patients

Exclusion Criteria:

  1. Suffering from severe mental illness
  2. Severe complications cannot tolerate surgery
  3. Simultaneous surgical treatment of other diseases is required
  4. History of gastric surgery (including ESD/EMR for gastric cancer)
  5. Tumors involving esophagus or duodenum were confirmed preoperatively
  6. Neoadjuvant therapy has been implemented
  7. Leather stomach
  8. Refusing laparoscopic surgery

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    indocyanine green labeled fluorescent laparoscopy

    The pathological staging

    Arm Description

    The experimental group was marked with indocyanine green, while the control group was not marked with indocyanine green

    They were grouped by different pathological stages

    Outcomes

    Primary Outcome Measures

    Three-year disease-free survival rate
    To evaluate the difference of 3-year disease-free survival rate between the experimental group and the control group

    Secondary Outcome Measures

    lymph node positive rate
    To evaluate the difference oflymph node positive rate between the experimental group and the control group
    Incidence of early complications
    The incidence of lymphatic leakage, shock and gastric stump leakage were used as secondary outcome measures
    operative mortality
    To investigate whether the mortality of laparoscopic proximal gastric cancer surgery marked with indocyanine green was lower than that of the control group

    Full Information

    First Posted
    April 25, 2022
    Last Updated
    May 26, 2022
    Sponsor
    Guangyong Zhang
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05369117
    Brief Title
    Application of Indocyanine Green Labeled Fluorescent Laparoscopy in Proximal Gastric Cancer
    Official Title
    To Evaluate Whether the Clinical Efficacy of Laparoscopic Lymph Node Dissection With Indocyanine Green Tracer is Better Than Without Indocyanine Green Tracer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    May 31, 2022 (Anticipated)
    Primary Completion Date
    May 1, 2027 (Anticipated)
    Study Completion Date
    May 6, 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Guangyong Zhang

    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
    Recently, laparoscopic gastrectomy has been gradually accepted by surgeons worldwide for gastric cancer treatment. Complete dissection of the lymph nodes and the establishment of the surgical margin are the most important considerations for curative gastric cancer surgery. Previous studies have demonstrated that indocyanine green (ICG)-traced laparoscopic gastrectomy significantly improves the completeness of lymph node dissection. However, it remains difficult to identify the tumor location intraoperatively for gastric cancers that are staged ≤T3. Here, the investigatorsinvestigated the feasibility of ICG fluorescence for lymph node mapping and tumor localization during totally laparoscopic distal gastrectomy.Preoperative and perioperative data from consecutive patients with gastric cancer who underwent a laparoscopic proximal gastrectomy were collected and analyzed. The investigators want to know if near-infrared fluorescence imaging with ICG can be successfully used in laparoscopic proximal gastrectomy, and if it contributes to both the completeness of D2 lymph node dissection and confirmation of the gastric transection line. The application of ICG labeled near infrared imaging fluorescence laparoscopic technology is still in the stage of exploration and experience accumulation, and it needs to be comprehensively evaluated through a large number of prospective randomized controlled studies.
    Detailed Description
    Recently, laparoscopic gastrectomy has been gradually accepted by surgeons worldwide for gastric cancer treatment. Complete dissection of the lymph nodes and the establishment of the surgical margin are the most important considerations for curative gastric cancer surgery. Previous studies have demonstrated that indocyanine green (ICG)-traced laparoscopic gastrectomy significantly improves the completeness of lymph node dissection. However, it remains difficult to identify the tumor location intraoperatively for gastric cancers that are staged ≤T3. Here, the investigatorsinvestigated the feasibility of ICG fluorescence for lymph node mapping and tumor localization during totally laparoscopic distal gastrectomy.Preoperative and perioperative data from consecutive patients with gastric cancer who underwent a laparoscopic proximal gastrectomy were collected and analyzed. The investigators want to know if near-infrared fluorescence imaging with ICG can be successfully used in laparoscopic proximal gastrectomy, and if it contributes to both the completeness of D2 lymph node dissection and confirmation of the gastric transection line. The application of ICG labeled near infrared imaging fluorescence laparoscopic technology is still in the stage of exploration and experience accumulation, and it needs to be comprehensively evaluated through a large number of prospective randomized controlled studies.By recruiting patients and signing informed consent, randomized control was used to divide patients into the experimental group (fluorescently labeled fluorescently laparoscopic proximal gastric cancer surgery) and the control group (fluorescently labeled fluorescently laparoscopic proximal gastric cancer surgery). In the experimental group, indocyanine green fluorescence labeling was performed under gastroscope before surgery and internal jugular vein puncture was performed routinely for better fluid replenishment after surgery. Lymph nodes and diseased stomach tissues were collected during operation. Postoperative assessment was made for ICU support, routine acid-suppressing therapy, prophylactic antibiotics, analgesia, and nausea suppression. The patients were followed up for 3 years. The primary outcome was 3-year disease-free survival, and the secondary outcome was lymph node positive rate, early complication rate and surgical mortality. The investigators plan to obtain more precise evidence-based medical evidence through this project.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Gastric Cancer
    Keywords
    Indocyanine green

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare Provider
    Allocation
    Randomized
    Enrollment
    1016 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    indocyanine green labeled fluorescent laparoscopy
    Arm Type
    Experimental
    Arm Description
    The experimental group was marked with indocyanine green, while the control group was not marked with indocyanine green
    Arm Title
    The pathological staging
    Arm Type
    Experimental
    Arm Description
    They were grouped by different pathological stages
    Intervention Type
    Behavioral
    Intervention Name(s)
    indocyanine green labeled fluorescent laparoscopy
    Intervention Description
    indocyanine green fluorescence labeling was performed under gastroscope before surgery and internal jugular vein puncture was performed routinely for better fluid replenishment after surgery
    Primary Outcome Measure Information:
    Title
    Three-year disease-free survival rate
    Description
    To evaluate the difference of 3-year disease-free survival rate between the experimental group and the control group
    Time Frame
    Through study completion,an average of 3 years
    Secondary Outcome Measure Information:
    Title
    lymph node positive rate
    Description
    To evaluate the difference oflymph node positive rate between the experimental group and the control group
    Time Frame
    up to 1 week
    Title
    Incidence of early complications
    Description
    The incidence of lymphatic leakage, shock and gastric stump leakage were used as secondary outcome measures
    Time Frame
    up to 1 week
    Title
    operative mortality
    Description
    To investigate whether the mortality of laparoscopic proximal gastric cancer surgery marked with indocyanine green was lower than that of the control group
    Time Frame
    up to 24 hours

    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 The primary gastric lesion was pathologically diagnosed as proximal gastric adenocarcinoma by endoscopic biopsy (papillary adenocarcinoma PAP, tubular adenocarcinoma TUB, mucinous adenocarcinoma MUC, signed-ring cell carcinoma SIG, poorly differentiated adenocarcinoma POR) Preoperative clinical staging was CT1-4A, N-/+, and M0, according to AJCC-8th TNM tumor staging No distant metastasis was found in preoperative examination, and the tumor did not directly invade pancreas, spleen or other adjacent organs ECOG physical status score 0/1 before surgery Preoperative ASA score I-III (7) Informed consent of patients Exclusion Criteria: Suffering from severe mental illness Severe complications cannot tolerate surgery Simultaneous surgical treatment of other diseases is required History of gastric surgery (including ESD/EMR for gastric cancer) Tumors involving esophagus or duodenum were confirmed preoperatively Neoadjuvant therapy has been implemented Leather stomach Refusing laparoscopic surgery

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Application of Indocyanine Green Labeled Fluorescent Laparoscopy in Proximal Gastric Cancer

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