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Fluorescence Imaging on the da Vinci Surgical System for Intra-operative Near Infrared Imaging of the Biliary Tree (up to 2-weeks Post-operatively)

Primary Purpose

Gallbladder Disease, Biliary Colic, Gallstones

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Indocyanine green (ICG)
Sponsored by
Intuitive Surgical
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Gallbladder Disease focused on measuring cholecystectomy, chronic right upper quadrant pain

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Informed consent
  • Ages of 18 to 80 years.
  • Symptoms consistent with gallbladder disease including biliary colic or chronic right upper quadrant pain.
  • Ultrasound confirming gallstones

Exclusion Criteria:

  • Acute cholecystitis
  • Biliary pancreatitis
  • Suspicion of common bile duct stones.
  • Pregnancy.
  • Previous upper abdominal open surgeries.
  • Severe lack of cooperation by patient due to psychological or severe systemic illness.
  • The presence of medical conditions contraindicating general anesthesia or standard surgical approaches.
  • Subject has a previous history of adverse reaction or allergy to ICG, iodine products (or excipient), shellfish or iodine dyes
  • Surgery converted to non-robotic procedures, such as open surgery or laparoscopic surgery

Sites / Locations

  • SS Antonio e Biagio e Cesare Arrigo
  • Hospital University Geneva

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ICG

Arm Description

Patient will received IV injection of ICG intra-operatively. Surgeon will view bile ducts under fluorescence imaging mode to see if ICG helps to identify biliary ducts.

Outcomes

Primary Outcome Measures

To identify biliary anatomy will be demonstrated by successful detection (90%) of one or more of the following biliary vessels: Cystic duct, common hepatic duct (CHD) or common bile duct (CBD).

Secondary Outcome Measures

observe and report peri-operative safety outcomes, including but not limited to incidence of adverse events and allergic reactions (rare according to the current knowledge and applications)

Full Information

First Posted
August 3, 2011
Last Updated
December 19, 2012
Sponsor
Intuitive Surgical
Collaborators
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria, University Hospital, Geneva
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1. Study Identification

Unique Protocol Identification Number
NCT01410734
Brief Title
Fluorescence Imaging on the da Vinci Surgical System for Intra-operative Near Infrared Imaging of the Biliary Tree (up to 2-weeks Post-operatively)
Official Title
A Prospective Investigation of the Use of the Fluorescence Imaging on the da Vinci Surgical System for Intra-operative Near Infrared Imaging of the Biliary Tree
Study Type
Interventional

2. Study Status

Record Verification Date
December 2012
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Intuitive Surgical
Collaborators
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria, University Hospital, Geneva

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators hypothesize that the da Vinci Fluorescence Imaging Vision System provides real-time endoscopic near infrared fluorescence imaging of the biliary anatomy as defined as identifying biliary vessels; either cystic duct, common hepatic duct (CHD) or common bile duct (CBD). Irradiation given to the patient during a classic cholangiography can be reduced.
Detailed Description
Up to 40 patients will be prospectively enrolled in this multi-centre (up to 5 centres) single arm study. After given consent, patients will undergo minimally invasive cholecystectomy with da Vinci Fluorescence Imaging using Indocynine green (ICG) and near infra-red light (NIR) to identify the surgically relevant anatomy of the biliary tree during this procedure. Efficacy endpoints The efficacy of the da Vinci Fluorescence Imaging Vision System to identify biliary anatomy will be demonstrated by successful detection (90%) of one or more of the following biliary vessels: Cystic duct, common hepatic duct (CHD) or common bile duct (CBD). Safety endpoints To observe and report peri-operative safety outcomes, including but not limited to incidence of adverse events and allergic reactions (rare according to the current knowledge and applications). Safety endpoints will be met by affirming the safety profile of the procedure, compared to currently available literature.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gallbladder Disease, Biliary Colic, Gallstones
Keywords
cholecystectomy, chronic right upper quadrant pain

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ICG
Arm Type
Experimental
Arm Description
Patient will received IV injection of ICG intra-operatively. Surgeon will view bile ducts under fluorescence imaging mode to see if ICG helps to identify biliary ducts.
Intervention Type
Drug
Intervention Name(s)
Indocyanine green (ICG)
Intervention Description
2.5mg indocyanine green (ICG) will be administerly (IV injection) 30 minutes before surgery
Primary Outcome Measure Information:
Title
To identify biliary anatomy will be demonstrated by successful detection (90%) of one or more of the following biliary vessels: Cystic duct, common hepatic duct (CHD) or common bile duct (CBD).
Time Frame
intra-operatively
Secondary Outcome Measure Information:
Title
observe and report peri-operative safety outcomes, including but not limited to incidence of adverse events and allergic reactions (rare according to the current knowledge and applications)
Time Frame
within 2 weeks post-operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed consent Ages of 18 to 80 years. Symptoms consistent with gallbladder disease including biliary colic or chronic right upper quadrant pain. Ultrasound confirming gallstones Exclusion Criteria: Acute cholecystitis Biliary pancreatitis Suspicion of common bile duct stones. Pregnancy. Previous upper abdominal open surgeries. Severe lack of cooperation by patient due to psychological or severe systemic illness. The presence of medical conditions contraindicating general anesthesia or standard surgical approaches. Subject has a previous history of adverse reaction or allergy to ICG, iodine products (or excipient), shellfish or iodine dyes Surgery converted to non-robotic procedures, such as open surgery or laparoscopic surgery
Facility Information:
Facility Name
SS Antonio e Biagio e Cesare Arrigo
City
Alessandria
State/Province
AL
ZIP/Postal Code
15100
Country
Italy
Facility Name
Hospital University Geneva
City
Geneva
Country
Switzerland

12. IPD Sharing Statement

Learn more about this trial

Fluorescence Imaging on the da Vinci Surgical System for Intra-operative Near Infrared Imaging of the Biliary Tree (up to 2-weeks Post-operatively)

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