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
About this trial
This is an interventional diagnostic trial for Peritoneal Carcinomatosis
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
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
NCT ID
NCT04352894
First Posted
April 14, 2020
Last Updated
April 17, 2020
Sponsor
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
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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