- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02680067
NIR Fluorescence Imaging of Lymphatic Transport Using ICG (NIR-ICG)
October 17, 2022 updated by: Christopher Ritchlin, University of Rochester
Near InfraRed Fluorescence Imaging of Lymphatic Transport Using Indocyanine Green
In this phase 1 study, the lymphatic transport will be examined using Near InfraRed Indocyanine Green fluorescence imaging (NIR-ICG) of the upper extremities in healthy individuals using a MultiSpectral Imaging System (MSImager).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Lymphedema from various etiologies (i.e.
infection, cancer, surgery, and rheumatoid arthritis) remains a major health concern.
Efforts to develop effective treatments for this condition have been limited by the absence of quantitative outcome measures for lymphatic function.
Published articles have supported the fact that human lymphatic contractions can be readily visualized after intradermal administration of micrograms of Indocyanine Green using laser-induced fluorescence.
The use of lasers imposes a risk of eye injury that requires protective eyewear.
To address the risk of laser-induced injury, an imaging system was developed by Drs.
Ronald Wood and Jay Reeder in a collaborative effort at the University of Rochester.
In place of a laser, this system utilizes a tungsten-halogen lamp fitted with a bandpass filter and a multispectral camera for real-time image acquisition and display.
This phase 1 study will examine the validity and reliability of this instrument to measure lymphatic transport, contractions, and pressure in the arms of healthy research subjects and establish baseline parameters for subsequent evaluation of rheumatoid arthritis patients in later studies.
Indocyanine Green is a dye that has been used clinically for over 50 years to evaluate hepatic clearance, cardiovascular function testing, and retinal angiography.
Indocyanine Green has typically been administered intravenously at concentrations of 2.5 mg/ml at total doses of 25 mg in adults.
In this study, intradermal administration of micrograms of Indocyanine Green will be used to establish useful dose ranges and concentrations.
The dosage regimen for this study is based on prior demonstrations in published articles of successful noninvasive imaging of lymphatic contractions after intradermal administration of microgram amounts of Indocyanine Green.
Study Type
Interventional
Enrollment (Actual)
23
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
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Rochester, New York, United States, 14642
- University of Rochester
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 89 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Ability to provide written informed consent
- Subjects can be either gender but must be at least 18 years old.
- Rheumatoid arthritis subjects may fulfill 2010 American College of Rheumatology criteria.
- Active rheumatoid arthritis subjects, with at least 2 tender or swollen joints.
- Subjects participating in the clearance arm of the study must not have ICG injections for at least 10 weeks.
Exclusion Criteria:
- Individuals with active systemic disorders or inflammatory conditions other than rheumatoid arthritis, (such as chronic infections with hepatitis B, hepatitis C or HIV) that would confound the study results.
- Known sensitivity to iodine because of residual iodide in Indocyanine Green
- Pregnant women should not participate.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: NON_RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Developmental arm - Healthy or rheumatoid arthritis subjects
Subjects in the developmental arm will have a minimum of two study visits to determine the optimal conditions for visualizing lymphatic transport in the upper extremities.
Concentrations of 0.1 mg/ml of Indocyanine Green (ICG) will be injected intradermally into the web spaces of the hands in both upper extremities.
Multispectral video and still images will be recorded using the MultiSpectral Imaging System (MSImager).
An ultrasound of the upper extremities may be performed after the ICG fluorescence is observed.
The exam will help identify the location of the lymphatic vessels and nodes in the areas fluoresced.
|
A trained physician will inject 0.1 ml of Indocyanine Green into the web spaces of the hands in both upper extremities.
Subjects may have up to five study visits to confirm feasibility, safety, and reproducibility.
Other Names:
Once the Indocyanine Green is injected, the contrast is expected to fluoresce underneath the MultiSpectral Imaging System.
Multispectral video and still images will be recorded at the study visits.
Other Names:
|
|
Experimental: Clearance arm - Healthy individuals
Subjects in the clearance arm will have an initial study visit that involves injections of 0.1 mg/ml of Indocyanine Green (ICG) intradermally into the web spaces of the hands in both upper extremities.
Multispectral video and still images will be recorded using the MultiSpectral Imaging System (MSImager).
Follow up imaging sessions will occur weekly for three weeks for a minimum of four study visits total.
|
A trained physician will inject 0.1 ml of Indocyanine Green into the web spaces of the hands in both upper extremities.
Subjects may have up to five study visits to confirm feasibility, safety, and reproducibility.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Contraction Rate
Time Frame: 36 months
|
The contraction rate is measured as lymphatic vessel contractions/min in the dominant lymphatic vessel efferent to the injection site using the MultiSpectral Imaging System (MSImager) that captures real time movies.
The MSImager software analyses the signal intensity to determine the contraction rate.
|
36 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lymphatic Pressure
Time Frame: 36 months
|
The lymphatic pressure is measured using a transparent cuff and the Multispectral Imaging System to determine indirect lymphatic pressure and recorded as mm Hg.
|
36 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clearance
Time Frame: 36 months
|
The change in Indocyanine Green signal intensity (arbitrary units) over time is measured by observing the fluorescence using the Multispectral Imaging System.
The MSImager software analyses the signal intensity.
|
36 months
|
|
Lymphatic Speed
Time Frame: 36 months
|
Speed with which an Indocyanine Green bolus moves through a lymphatic vessel recorded as mm -sec-1 using the Multispectral Imaging System.
The MSImager software analyses the signal speed.
|
36 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 8, 2015
Primary Completion (Actual)
July 1, 2022
Study Completion (Actual)
July 1, 2022
Study Registration Dates
First Submitted
December 7, 2015
First Submitted That Met QC Criteria
February 8, 2016
First Posted (Estimate)
February 11, 2016
Study Record Updates
Last Update Posted (Actual)
October 18, 2022
Last Update Submitted That Met QC Criteria
October 17, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RSRB 54038
- R01AR056702 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Information of any type may be shared with researchers at other institutions.
Subjects will be made aware of this in the informed consent form.
Study Data/Documents
-
Arthritis Research & Therapy Publication
Information comments: Lymphatic imaging to assess rheumatoid flare: mechanistic insights and biomarker potential.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Yes
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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