Fluorescent Cholangiography and Bile Duct Stones
Primary Purpose
Gall Stones, Common Bile Duct
Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Presence of bile duct stones
Non-presence of bile duct stones
Sponsored by
About this trial
This is an interventional diagnostic trial for Gall Stones, Common Bile Duct focused on measuring fluorescence, cholangiography, cholecystectomy, laparoscopic
Eligibility Criteria
Inclusion criteria
- Patients suspected of having bile duct stones by either blood samples, MRCP or medical history (see definitions)
- Patient age ≥ 18 years
- Preoperative MRCP
- Operation performed by a project surgeon
Exclusion criteria
- Open cholecystectomy (including conversion from laparoscopic to open)
- Acute cholecytitis or cholangitis
- Pancreatitis
- Iodine or indocyanine green allergy
- Liver or renal insufficiency
- Thyrotoxicosis
- Cholecystectomy not the primary surgical procedure
- Pregnancy or lactation
- Legally incompetent for any reason
- Withdrawal of inclusion consent at any time
Sites / Locations
- Hvidovre University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
MRCP positive
MRCP negative
Arm Description
Outcomes
Primary Outcome Measures
Sensitivity and specificity
Sensitivity and specificity of visualization of bile duct stones by intraoperative fluorescent cholangiography
Secondary Outcome Measures
Visualization
Visualization of the extrahepatic bile ducts
Full Information
NCT ID
NCT03530241
First Posted
May 8, 2018
Last Updated
April 1, 2020
Sponsor
Hvidovre University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03530241
Brief Title
Fluorescent Cholangiography and Bile Duct Stones
Official Title
Sensitivity and Specificity of Fluorescent Cholangiography to Detect Bile Duct Stones in Patients Undergoing Laparoscopic Cholecystectomy
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 25, 2019 (Actual)
Primary Completion Date
October 31, 2020 (Anticipated)
Study Completion Date
August 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hvidovre University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Background. X-ray cholangiography has a high sensitivity and specificity of detecting bile duct stones and is the gold standard. There are no studies describing the sensitivity and specificity of IFC for bile duct stone detection.
Research question. What is the sensitivity of IFC to visualize bile duct stones? Method. Prospective study with 40 patients undergoing planned laparoscopic cholecystectomy with preoperative magnetic resonance cholangiopancreatography (MRCP) (gold standard) and intraoperative IFC, X-ray cholangiography and choledochuscopy in that order.
Primary outcome. Sensitivity of visualization of bile duct stone by fluorescent cholangiography and secondary outcome is visualization of anatomy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gall Stones, Common Bile Duct
Keywords
fluorescence, cholangiography, cholecystectomy, laparoscopic
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
MRCP positive
Arm Type
Experimental
Arm Title
MRCP negative
Arm Type
Active Comparator
Intervention Type
Diagnostic Test
Intervention Name(s)
Presence of bile duct stones
Intervention Description
MRCP verified gall stones in the bile ducts
Intervention Type
Diagnostic Test
Intervention Name(s)
Non-presence of bile duct stones
Intervention Description
MRCP without bile duct stones
Primary Outcome Measure Information:
Title
Sensitivity and specificity
Description
Sensitivity and specificity of visualization of bile duct stones by intraoperative fluorescent cholangiography
Time Frame
120mins
Secondary Outcome Measure Information:
Title
Visualization
Description
Visualization of the extrahepatic bile ducts
Time Frame
120mins
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria
Patients suspected of having bile duct stones by either blood samples, MRCP or medical history (see definitions)
Patient age ≥ 18 years
Preoperative MRCP
Operation performed by a project surgeon
Exclusion criteria
Open cholecystectomy (including conversion from laparoscopic to open)
Acute cholecytitis or cholangitis
Pancreatitis
Iodine or indocyanine green allergy
Liver or renal insufficiency
Thyrotoxicosis
Cholecystectomy not the primary surgical procedure
Pregnancy or lactation
Legally incompetent for any reason
Withdrawal of inclusion consent at any time
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars L Lehrskov, MD
Organizational Affiliation
Hvidovre University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hvidovre University Hospital
City
Holte
State/Province
Danmark
ZIP/Postal Code
2840
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Fluorescent Cholangiography and Bile Duct Stones
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