Fluorescence Imaging + ICG Dye for Use in the Visual Diagnosis of Endometriosis (FIREFLY)
Primary Purpose
Endometriosis
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Participants will receive ICG Dye
Sponsored by
About this trial
This is an interventional diagnostic trial for Endometriosis focused on measuring Endometriosis, Robotic Surgery, Diagnostic Imaging
Eligibility Criteria
Inclusion Criteria:
- Be premenopausal (menopause is defined as amenorrhea lasting one year or longer)
- Have symptoms consistent with endometriosis, including the presence of one or more of the following: dysmenorrhea; dyspareunia; chronic pelvic pain (>6 months duration); pressure on the bladder or rectum causing difficult or painful bowel movements; infertility.
- Be willing to undergo planned da Vinci Endometriosis Resection Procedure
Exclusion Criteria:
- Known or suspected allergy to iodine, shellfish, or ICG dye
- Presence of medical conditions contraindicating general anesthesia or standard laparoscopic/ robotic surgery
- Active pelvic infection
- Previous history of radiation therapy to the pelvis
- Known or suspected pregnancy
- Presence of anatomy unsuitable for laparoscopic surgery
- Previously undiagnosed intra-abdominal or pelvic malignancy
- Inability of patient to tolerate Trendelenberg position or pneumoperitoneum
Sites / Locations
- Florida Hospital Celebration Health
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
+ ICG Dye (Firefly)
Arm Description
Participants will receive ICG Dye
Outcomes
Primary Outcome Measures
Quality of fluorescence imaging using + ICG dye (Firefly).
Quality is defined by the investigators perception of accuracy of visual diagnosis and how clear are the the resultant images used for visualization and mapping of lesions. The quality of the fluorescence imaging + ICG dye (Firefly) will be compared to standard white light imaging in 2D and 3D for accurate visual diagnosis of endometriosis during a da Vinci endometriosis resection procedure
Secondary Outcome Measures
Quality of Life
Quality of Life (QOL) will be captured by utilizing the validated questionnaire SF-36 short form, administered at three time-points: pre-operative, at 3-months post-operative, and at 6-months post-operative. The QOL aspects examined with the SF-36 include vitality, mental health physical functioning, bodily pain, general health perceptions, as well as physical, emotional, and social role functioning.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02038985
Brief Title
Fluorescence Imaging + ICG Dye for Use in the Visual Diagnosis of Endometriosis
Acronym
FIREFLY
Official Title
An Evaluation of Fluorescence Imaging + ICG Dye (Firefly) for Use in the Visual Diagnosis of Endometriosis: A Prospective Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Terminated
Why Stopped
Lack of funding
Study Start Date
June 2013 (Actual)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
August 16, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AdventHealth
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the use of fluorescence imaging + Indocyanine Green (ICG) dye ("Firefly"), compared to standard white light imaging in 2D and 3D, for accurate visual diagnosis of endometriosis during a da Vinci robotically guided endometriosis resection procedure.
Detailed Description
Fluorescence imaging has been used for visualization of tissue perfusion in colorectal surgery, detection of pathologic primary and metastatic tumors, and measurement of graft patency in cardiovascular surgery. The da Vinci® Firefly Imaging System, through the use of fluorescence imaging, allows surgeons to view high-resolution near infrared images of blood flow and tissue perfusion in real-time during robotic-assisted surgical procedures, such as during a robotic-assisted endometriosis resection.
Using standard white light imaging, endometriotic lesions can appear red and vascular, white and scarred, black, brown, yellow, or almost any color; atypical implants are clear and can seem like normal tissue. However, there are some published reports demonstrating that the lesions of endometriosis are hypervascular and may be visualized radiographically on the basis of this pathologic feature. Because the individual lesions of endometriosis can vary significantly in their appearance under standard white light, using the hypervascular characteristic of this disease along with the Firefly technology may provide consistency in intraoperative visual diagnosis, and thus may aid the detection and resection of endometriosis.
The ability to accurately visualize all the lesions of endometriosis, typical and atypical in appearance, and thus facilitate complete resection of the disease, may have a significant impact on symptomatic relief and disease recurrence. The Firefly Imaging System of fluorescence imaging + ICG dye may allow for more accurate visual diagnosis of endometriosis during a robotic-assisted endometriosis resection procedure, and therefore may have a positive impact for patients with this disease.
This is a prospective, comparison, single-center, observational study to evaluate fluorescence imaging + ICG dye (Firefly), compared to standard white light imaging in 2D and 3D, for accurate visual diagnosis of endometriosis during a da Vinci endometriosis resection procedure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis
Keywords
Endometriosis, Robotic Surgery, Diagnostic Imaging
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Actual)
8. Arms, Groups, and Interventions
Arm Title
+ ICG Dye (Firefly)
Arm Type
Other
Arm Description
Participants will receive ICG Dye
Intervention Type
Other
Intervention Name(s)
Participants will receive ICG Dye
Intervention Description
Participants will receive ICG Dye preoperatively for use in the Visual Diagnosis of Endometriosis
Primary Outcome Measure Information:
Title
Quality of fluorescence imaging using + ICG dye (Firefly).
Description
Quality is defined by the investigators perception of accuracy of visual diagnosis and how clear are the the resultant images used for visualization and mapping of lesions. The quality of the fluorescence imaging + ICG dye (Firefly) will be compared to standard white light imaging in 2D and 3D for accurate visual diagnosis of endometriosis during a da Vinci endometriosis resection procedure
Time Frame
1 hour
Secondary Outcome Measure Information:
Title
Quality of Life
Description
Quality of Life (QOL) will be captured by utilizing the validated questionnaire SF-36 short form, administered at three time-points: pre-operative, at 3-months post-operative, and at 6-months post-operative. The QOL aspects examined with the SF-36 include vitality, mental health physical functioning, bodily pain, general health perceptions, as well as physical, emotional, and social role functioning.
Time Frame
3 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Be premenopausal (menopause is defined as amenorrhea lasting one year or longer)
Have symptoms consistent with endometriosis, including the presence of one or more of the following: dysmenorrhea; dyspareunia; chronic pelvic pain (>6 months duration); pressure on the bladder or rectum causing difficult or painful bowel movements; infertility.
Be willing to undergo planned da Vinci Endometriosis Resection Procedure
Exclusion Criteria:
Known or suspected allergy to iodine, shellfish, or ICG dye
Presence of medical conditions contraindicating general anesthesia or standard laparoscopic/ robotic surgery
Active pelvic infection
Previous history of radiation therapy to the pelvis
Known or suspected pregnancy
Presence of anatomy unsuitable for laparoscopic surgery
Previously undiagnosed intra-abdominal or pelvic malignancy
Inability of patient to tolerate Trendelenberg position or pneumoperitoneum
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aileen Caceres, MD
Organizational Affiliation
Florida Hospital Celebration Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Florida Hospital Celebration Health
City
Celebration
State/Province
Florida
ZIP/Postal Code
34747
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Fluorescence Imaging + ICG Dye for Use in the Visual Diagnosis of Endometriosis
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