A Study of Perfusion of Colorectal Anastomosis Using FLuorescence AnGiography (FLAG-trial) (FLAG)
Primary Purpose
Rectal Cancer, Sigmoid Cancer
Status
Completed
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Fluorescence angiography with indocianyne green
Sponsored by
About this trial
This is an interventional treatment trial for Rectal Cancer focused on measuring fluorescence angiography, indocyanine green, anastomotic leakage
Eligibility Criteria
Inclusion Criteria:
- Have a planned circular stapled colorectal anastomosis
- Have signed an approved informed consent form for the study
Exclusion Criteria:
- Has known allergy or history of adverse reaction to indocianyne green, iodine or iodine dyes.
Sites / Locations
- State Scientific Centre of Coloproctology
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
ICG group
Standard
Arm Description
A sigmoid and rectum resection with colorectal anastomosis will be performed according to the surgeons standard practice with the addition of intraoperative imaging using fluorescence angiography with indocianyne green to assess colon and rectal tissue perfusion.
A sigmoid and rectum resection with colorectal anastomosis will be performed according to the surgeons standard practice.
Outcomes
Primary Outcome Measures
Anastomotic Leak Rate
Secondary Outcome Measures
Full Information
NCT ID
NCT03390517
First Posted
December 27, 2017
Last Updated
September 24, 2019
Sponsor
State Scientific Centre of Coloproctology, Russian Federation
1. Study Identification
Unique Protocol Identification Number
NCT03390517
Brief Title
A Study of Perfusion of Colorectal Anastomosis Using FLuorescence AnGiography (FLAG-trial)
Acronym
FLAG
Official Title
A Study of Perfusion of Colorectal Anastomosis Using FLuorescence AnGiography (FLAG-trial)
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
November 9, 2017 (Actual)
Primary Completion Date
August 22, 2019 (Actual)
Study Completion Date
September 22, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
State Scientific Centre of Coloproctology, Russian Federation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a randomized, controlled, parallel study to determine the difference in post-operative anastomotic leak rate of colorectal anastomosis where colon and rectal tissue perfusion is evaluated using fluorescence angiography with indocyanine green and without this method.
Detailed Description
The design involves random allocation of eligible patients to operation with colorectal anastomosis and intraoperative fluorescence angiography with indocyanine green and operation alone. After surgery on 7-8 POD patients are examined to two sides X-Ray proctography performed by introducing 100 ml of water-soluble liquid contrast material through the anus over the anastomotic line by a Foley catheter for diagnosis of anastomotic leakage.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer, Sigmoid Cancer
Keywords
fluorescence angiography, indocyanine green, anastomotic leakage
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
377 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ICG group
Arm Type
Experimental
Arm Description
A sigmoid and rectum resection with colorectal anastomosis will be performed according to the surgeons standard practice with the addition of intraoperative imaging using fluorescence angiography with indocianyne green to assess colon and rectal tissue perfusion.
Arm Title
Standard
Arm Type
No Intervention
Arm Description
A sigmoid and rectum resection with colorectal anastomosis will be performed according to the surgeons standard practice.
Intervention Type
Device
Intervention Name(s)
Fluorescence angiography with indocianyne green
Intervention Description
The fluorescence angiography was performed after mobilization of the bowel, transection of the rectum, division of the rectal and colon mesentery and central vessels, before specimen extraction or resection and creation of the anastomosis. This site was selected by the surgeon using his or her best judgment and typical standard of care assessment. After this selection, the anesthesiologist administered a bolus of 1 to 2 ml indocianyne green intravenously. Perfusion of the colon was visualized and assessed via fluorescence angiography and the line of demarcation between perfused and nonperfused tissue was noted and compared with the initial planned transection point.
Primary Outcome Measure Information:
Title
Anastomotic Leak Rate
Time Frame
0 to 30 days
10. Eligibility
Sex
All
Gender Based
Yes
Gender Eligibility Description
18 years and older
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Have a planned circular stapled colorectal anastomosis
Have signed an approved informed consent form for the study
Exclusion Criteria:
Has known allergy or history of adverse reaction to indocianyne green, iodine or iodine dyes.
Facility Information:
Facility Name
State Scientific Centre of Coloproctology
City
Moscow
ZIP/Postal Code
123423
Country
Russian Federation
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
A Study of Perfusion of Colorectal Anastomosis Using FLuorescence AnGiography (FLAG-trial)
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