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Intraoperative ICG Fluorescence Imaging for Peritoneal Carcinomatosis Detection

Primary Purpose

Peritoneal Carcinomatosis, Gastric Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Fluorescence guided peritoneal exploration
Sponsored by
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Peritoneal Carcinomatosis

Eligibility Criteria

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

Inclusion Criteria:

  1. Age of ≥18years
  2. Ability to provide written informed consent
  3. Histologically confirmed gastric adenocarcinoma or oesophago-gastric junction adenocarcinoma Siewert 2 and 3
  4. cT>1
  5. cM0 (clinical staging: no metastases)
  6. Staging laparoscopy is indicated by the internal work-up protocol
  7. Staging laparoscopy is in accordance with NCCN (National Comprehensive Cancer Network) guidelines

Exclusion Criteria:

  1. Pregnancy
  2. Iodine allergy/sensibility
  3. Clinical P1 (defined as high probability of peritoneal carcinomatosis at imaging)
  4. Investigator judgement that the patient should not participate for any reason

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    fluorescence guided peritoneal exploration

    Arm Description

    Indocyanine green (ICG) intravenous injection and peritoneal exploration with technology able to detect fluorescence generated by ICG

    Outcomes

    Primary Outcome Measures

    Best modality of ICG injection
    best timing of injection

    Secondary Outcome Measures

    Sensitivity of ICG fluorescence
    As compared with white light

    Full Information

    First Posted
    April 14, 2020
    Last Updated
    April 17, 2020
    Sponsor
    Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04352894
    Brief Title
    Intraoperative ICG Fluorescence Imaging for Peritoneal Carcinomatosis Detection
    Official Title
    Indocyanine Green Fluorescence Detection of Peritoneal Carcinomatosis During Staging Laparoscopy for Gastric Cancer: Protocol for a Prospective Multicentric Single Arm Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 2020 (Anticipated)
    Primary Completion Date
    September 2021 (Anticipated)
    Study Completion Date
    September 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Background. Peritoneal carcinomatosis is a frequent and deadly localization of gastric cancer. Available imaging techniques have a low accuracy in detecting small peritoneal nodules, and direct laparoscopic visualization may fail too. A more accurate staging technique would be advantageous for individualization of therapeutic path. Indocyanine Green (ICG) fluorescence imaging has been reported as a tool for visualizing small peritoneal seedings due to the "enhanced permeability and retention" (EPR) effect of cancer nodules. Aim. To explore the feasibility and effectiveness of fluorescence-enhanced peritoneal carcinomatosis detection in patients with gastric cancer undergoing staging laparoscopy. Methods. This prospective, multicentric, single arm study will include patients with gastric cancer, without a radiological suspicion of peritoneal carcinomatosis, undergoing staging laparoscopy. An intravenous injection of ICG is given at different dosage and at different timepoints before the intervention. During the staging laparoscopy, the abdominal cavity exploration is performed using standard white-light, and subsequently using fluorescence imaging. Suspicious nodules are harvested, until a maximum of 5 per patient, and sent for definitive histological examination. Peritoneal washing is also harvested for cytologic assessment in all cases. The eventual benefit of fluorescence imaging in terms of additional peritoneal lesions that were not detected during standard white-light imaging is evaluated. Discussion. This study will establish if fluorescence imaging increases sensitivity and/or specificity of staging laparoscopy in detecting peritoneal carcinomatosis from gastric cancer. Improved accuracy may translate in better care path selection.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Peritoneal Carcinomatosis, Gastric Cancer

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    fluorescence guided peritoneal exploration
    Arm Type
    Experimental
    Arm Description
    Indocyanine green (ICG) intravenous injection and peritoneal exploration with technology able to detect fluorescence generated by ICG
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Fluorescence guided peritoneal exploration
    Intervention Description
    Intravenous injection of ICG
    Primary Outcome Measure Information:
    Title
    Best modality of ICG injection
    Description
    best timing of injection
    Time Frame
    intra-operative assessment
    Secondary Outcome Measure Information:
    Title
    Sensitivity of ICG fluorescence
    Description
    As compared with white light
    Time Frame
    intra-operative assessment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age of ≥18years Ability to provide written informed consent Histologically confirmed gastric adenocarcinoma or oesophago-gastric junction adenocarcinoma Siewert 2 and 3 cT>1 cM0 (clinical staging: no metastases) Staging laparoscopy is indicated by the internal work-up protocol Staging laparoscopy is in accordance with NCCN (National Comprehensive Cancer Network) guidelines Exclusion Criteria: Pregnancy Iodine allergy/sensibility Clinical P1 (defined as high probability of peritoneal carcinomatosis at imaging) Investigator judgement that the patient should not participate for any reason
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Gian Luca Baiocchi, Prof.
    Phone
    ++39 338 5949921
    Email
    gianluca.baiocchi@unibs.it
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Gian Luca Baiocchi, Prof
    Organizational Affiliation
    ASST Spedali Civili, University of Brescia
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Intraoperative ICG Fluorescence Imaging for Peritoneal Carcinomatosis Detection

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