Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy (NIRF-C)
Primary Purpose
Cholecystitis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Injection of indocyanine green (ICG)
Near Infrared Cholangiography Fluorescence (NIRF-C)
Sponsored by
About this trial
This is an interventional diagnostic trial for Cholecystitis focused on measuring cholecystectomy, cholecystitis
Eligibility Criteria
Inclusion Criteria:
- Age 18-89
- Planned laparoscopic cholecystectomy
Exclusion Criteria:
- Inability to provide informed consent
- Pregnant
- Allergy to ICG, iodine, and/or shellfish
- Acute cholecystitis, cholangitis, and/or cirrhosis (main study)
- Lactating
Sites / Locations
- The Ohio State University Wexner Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
NIRF-C
Arm Description
Each subject enrolled in this study will undergo near-infrared cholangiography fluorescence (NIRF-C) and standard of care intraoperative cholangiography. 2.5 mg of indocyanine green is injected 30-60 minutes prior to surgery. Visualization of the biliary tree during surgery is achieved with a near-infrared light source and camera.
Outcomes
Primary Outcome Measures
Complications Related to ICG
A patient's negative reaction to indocyanine green (ICG) will be monitored from the time of injection through the 2 week post-operative follow-up visit.
Secondary Outcome Measures
Incidence of Anatomic Identification With NIRF-C
Incidence of anatomic identification with NIRF-C and intraoperative cholangiography.
Time to Complete NIRF-C and IOC
The time required to complete NIRF-C and intraoperative cholangiography will be analyzed.
Full Information
NCT ID
NCT02070640
First Posted
February 21, 2014
Last Updated
September 22, 2015
Sponsor
Ohio State University
Collaborators
Stryker Instruments, Society of American Gastrointestinal and Endoscopic Surgeons
1. Study Identification
Unique Protocol Identification Number
NCT02070640
Brief Title
Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy
Acronym
NIRF-C
Official Title
Near Infrared Fluorescence Cholangiography During Cholecystectomy
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
August 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University
Collaborators
Stryker Instruments, Society of American Gastrointestinal and Endoscopic Surgeons
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate an imaging system using Indocyanine Green (ICG) to assist in real-time identification of anatomy during cholecystectomy (gallbladder removal). We propose to define the effectiveness of NIRF-C in identifying the cystic duct junction during cholecystectomy.
Detailed Description
This study is designed to determine the clinical utility of intravenous indocyanine green (ICG) injection pre-operatively for cholecystectomy, followed by visualizuation of the biliary tree with a near-infrared light source and camera. Testing will be done during an abdominal surgery which requires gallbladder removal. Subjects will be recruited during consult for their surgical procedure. The study itself will take an estimated 5 minutes during the procedure. 2.5mg of ICG will be injected intravenously 60-30 minutes before surgery, and following perfusion of the biliary tree, images will be recorded and visibility of the appropriate anatomy will be assessed using a near-infrared light source and camera. If fluorescence has faded prior to adequate visualization, a repeat dose of 2.5mg IV ICG may be given. Following the completion of imaging, the standard procedure for cholecystectomy will be performed including intraoperative cholangiography (IOC), which is standard of care. Subject post-operative recovery will be monitored for the duration of their hospital stay. Adverse events will be monitored at the patient's routine follow up visit.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cholecystitis
Keywords
cholecystectomy, cholecystitis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
99 (Actual)
8. Arms, Groups, and Interventions
Arm Title
NIRF-C
Arm Type
Experimental
Arm Description
Each subject enrolled in this study will undergo near-infrared cholangiography fluorescence (NIRF-C) and standard of care intraoperative cholangiography. 2.5 mg of indocyanine green is injected 30-60 minutes prior to surgery. Visualization of the biliary tree during surgery is achieved with a near-infrared light source and camera.
Intervention Type
Drug
Intervention Name(s)
Injection of indocyanine green (ICG)
Intervention Description
2.5 mg of of ICG will be injected intravenously 60-30 minutes prior to surgery in order to visualize the biliary tree using a near-infrared light source and camera. An additional 2.5 mg of IV ICG may be given intraoperatively if fluorescence has faded prior to visualization.
Intervention Type
Device
Intervention Name(s)
Near Infrared Cholangiography Fluorescence (NIRF-C)
Other Intervention Name(s)
Stryker 1488 Camera System, Stryker L9000 Light Source, Stryker 1488 Coupler, Stryker 10mm Ideal Eyes Laparoscope (0 and 30 degree)
Intervention Description
These devices are used to identify anatomy, using infrared light that causes the ICG to fluoresce.
Primary Outcome Measure Information:
Title
Complications Related to ICG
Description
A patient's negative reaction to indocyanine green (ICG) will be monitored from the time of injection through the 2 week post-operative follow-up visit.
Time Frame
From time of injection to 1st post-op follow-up
Secondary Outcome Measure Information:
Title
Incidence of Anatomic Identification With NIRF-C
Description
Incidence of anatomic identification with NIRF-C and intraoperative cholangiography.
Time Frame
Intraoperative
Title
Time to Complete NIRF-C and IOC
Description
The time required to complete NIRF-C and intraoperative cholangiography will be analyzed.
Time Frame
Intraoperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18-89
Planned laparoscopic cholecystectomy
Exclusion Criteria:
Inability to provide informed consent
Pregnant
Allergy to ICG, iodine, and/or shellfish
Acute cholecystitis, cholangitis, and/or cirrhosis (main study)
Lactating
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vimal K Narula, MD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Ohio State University Wexner Medical Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43214
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Near Infrared Fluorescence Cholangiography (NIRF-C) During Cholecystectomy
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