Evaluation of the Capacity of a Camera to Identify Signs of Arteriosclerosis in Retinal Arterioles
Primary Purpose
Arteriosclerosis
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
MHRC: Metabolic Hyperspectral Retinal Camera
Sponsored by
About this trial
This is an interventional diagnostic trial for Arteriosclerosis
Eligibility Criteria
Inclusion Criteria:
Subjects suffering from arteriosclerosis:
- myocardial infarction
- coronary angiography showing at least one coronary stenosis (more than 50%)
- and/or coronary angioplasty
- and/or coronary bypass.
Healthy control subjects:
- absence of a medical history of cardiovascular disease
- absence of medical history of cerebrovascular disease
- absence of a medical history of peripheral arterial disease
Exclusion Criteria:
Healthy control subjects:
- myocardial infarction or angina
- known coronary stenosis
- coronary angioplasty history or coronary bypass surgery
- stroke or transient ischemic attack history
- peripheral arterial disease history
- active smoking or history smoking in the past 5 years
- diabetes mellitus
- familial hypercholesterolemia
- poorly controlled hypertension (systolic blood pressure ≥150 mm Hg)
All subjects:
- medium or high opacity of the lens (which interferes with the MHRC imaging)
- bleeding in the vitreous (which interfere with MHRC imaging)
- presence of venous occlusion, age-related macular degeneration or glaucoma
- pupillary dilation inadequate or contra-indicated
- deficient visual fixation
- refractive error outside of the range -9 to +9
- inability to obtain satisfactory images with the MHRC
Sites / Locations
- Montreal Heart InstituteRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Arteriosclerosis
Healthy controls
Arm Description
Hyperspectral camera for arteriosclerosis Diagnostic
Hyperspectral camera for healthy control Diagnostic
Outcomes
Primary Outcome Measures
Spectral intensity measures to visible and near infrared light around retinal arterioles in 30 patients with clearly defined atherosclerosis and 30 controls.
Data will be aggregated for all arterioles identified in retinal image to produce a single outcome
Secondary Outcome Measures
Full Information
NCT ID
NCT02849405
First Posted
July 14, 2016
Last Updated
March 1, 2018
Sponsor
Jean-Claude Tardif
Collaborators
Montreal Heart Institute, Polytechnique Montréal
1. Study Identification
Unique Protocol Identification Number
NCT02849405
Brief Title
Evaluation of the Capacity of a Camera to Identify Signs of Arteriosclerosis in Retinal Arterioles
Official Title
Preliminary Evaluation of the Capacity of a Metabolic Hyperspectral Retinal Camera (MHRC) to Identify an Arteriosclerosis Spectral Signature in Retinal Arterioles
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Unknown status
Study Start Date
December 21, 2016 (Actual)
Primary Completion Date
October 2018 (Anticipated)
Study Completion Date
October 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jean-Claude Tardif
Collaborators
Montreal Heart Institute, Polytechnique Montréal
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Arteriosclerosis is a degenerative and dysmetabolic disease of the arterial walls. It is known to be the principal cause of coronary artery disease (CAD). Arteriosclerosis has an impact on the entire vascularization including the microvascularization. The retina is a nervous tissue that is supported by microvascularization. Therefore, systemic diseases that affect the nervous or the cardiovascular system are susceptible to have manifestations in the retina. Retinal signs associated to the risks to develop CAD (qualitative appreciation; diameter and appearance of arterioles) have been suggested. A quantitative approach would strengthen the interpretation of these evaluations.
The Metabolic Hyperspectral Retinal Camera (MHRC) - the experimental instrument - has the capacity to identify and quantify a variety of biomolecules specific to the retina and the optic nerve.
The purpose of this pilot study is to determine if the MHRC has the capacity to detect a specific hyperspectral signature in the retinal arterioles of subjects suffering from arteriosclerosis.
Detailed Description
In this pilot study, the main goal is to evaluate the capacity of the Metabolic Hyperspectral Retinal Camera (MHRC) - the experimental instrument - to identify the presence of a specific hyperspectral signature in the retinal arterioles of subjects suffering from arteriosclerosis while this signature should not be present in the retinal arterioles of control subjects considered healthy and without arteriosclerosis risk factors. The study is open, non-controlled and without randomization or placebo.
30 subjects of each group will be enrolled in the study for a total of 60 subjects. Recruitment will take place at the Montreal Heart Institute (Montreal, Quebec, Canada) and will be led by the research team of the Principal Investigator. Specific inclusion/exclusion criteria will differentiate subjects in each group. Once subjects fitting the inclusion/exclusion criteria will be identified, they will be enrolled and asked to sign the informed consent form approved by the Research Ethics and New Technology Development Committee (Montreal Heart Institute).
Following this step, an ophthalmic examination will be performed. During this examination, both eyes will be evaluated in order to detect the presence of eye pathologies (advanced cataracts, venous occlusion, age-related macular degeneration or glaucoma) that could interfere with the analysis of the MHRC optical imaging results. The ophthalmic examination consists first of a slit-lamp evaluation and secondly of an optic coherence tomography (OCT) plus a color image of the fundus (standard instruments commonly used in ophthalmology clinics) following the instillation of eye drops to dilate the pupils. The whole examination should last 45 minutes (it takes 15 to 20 minutes for the pupil to be sufficiently dilated to carry out the examinations). If the ophthalmic examination does not reveal any of the exclusion criteria, in the next minutes, the subject will be asked to undergo the baseline MHRC examination. This baseline imaging session will last a maximum of 15 minutes.
All data according to the light signal spectrum will be analyzed subsequently. Only depersonalized data, identified solely by the subject number, will be used by the investigators.
Risks associated to the subject's participation in this research project have been evaluated. Pupil dilation will be necessary to obtain quality images of the retina using conventional imaging techniques (OCT and fundus) and with the MHRC. The subject's pupils will remain dilated for 4 to 6 hours afterward, which may cause significant glare in areas where light is strong.. The MHRC is a research instrument which images the retina non-invasively and Health Canada authorization has been obtained for its use in the context of this study. The only foreseeable harm connected to its use is discomfort connected to the injection of light into the eye. The power of the monochromatic light source has been calculated to be well below the recommended exposure limits.. Very rigorous verifications were made according to the parameters fixed by the "American National Standard for safe use of laser" (ANSI 136.1) for laser radiation exposure.
Finally, all conflicts of interested are declared in the protocol and the informed consent form. Measures are in place to mitigate them in order to maintain research and data analysis integrity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arteriosclerosis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Arteriosclerosis
Arm Type
Other
Arm Description
Hyperspectral camera for arteriosclerosis Diagnostic
Arm Title
Healthy controls
Arm Type
Other
Arm Description
Hyperspectral camera for healthy control Diagnostic
Intervention Type
Device
Intervention Name(s)
MHRC: Metabolic Hyperspectral Retinal Camera
Intervention Description
Comparison of hyperspectral signature of retinal arterioles between subjects suffering from arteriosclerosis and healthy control subjects.
Primary Outcome Measure Information:
Title
Spectral intensity measures to visible and near infrared light around retinal arterioles in 30 patients with clearly defined atherosclerosis and 30 controls.
Description
Data will be aggregated for all arterioles identified in retinal image to produce a single outcome
Time Frame
1 Year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Subjects suffering from arteriosclerosis:
myocardial infarction
coronary angiography showing at least one coronary stenosis (more than 50%)
and/or coronary angioplasty
and/or coronary bypass.
Healthy control subjects:
absence of a medical history of cardiovascular disease
absence of medical history of cerebrovascular disease
absence of a medical history of peripheral arterial disease
Exclusion Criteria:
Healthy control subjects:
myocardial infarction or angina
known coronary stenosis
coronary angioplasty history or coronary bypass surgery
stroke or transient ischemic attack history
peripheral arterial disease history
active smoking or history smoking in the past 5 years
diabetes mellitus
familial hypercholesterolemia
poorly controlled hypertension (systolic blood pressure ≥150 mm Hg)
All subjects:
medium or high opacity of the lens (which interferes with the MHRC imaging)
bleeding in the vitreous (which interfere with MHRC imaging)
presence of venous occlusion, age-related macular degeneration or glaucoma
pupillary dilation inadequate or contra-indicated
deficient visual fixation
refractive error outside of the range -9 to +9
inability to obtain satisfactory images with the MHRC
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David Lapointe, M.Sc.
Phone
438-828-1675
Email
dlapointe@optinadx.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Philippe Sylvestre, Eng., Ph.D.
Phone
514-966-0325
Email
j-psylvestre@optinadx.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Claude Tardif, MD
Organizational Affiliation
Montreal Heart Insitute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montreal Heart Institute
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H1T 1C8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gilles Lefebvre
Phone
5143763330
Email
gilles.lefebvre@icm-mhi.org
First Name & Middle Initial & Last Name & Degree
Jean-Claude Tardif, M.D.
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
17429471
Citation
Delori FC, Webb RH, Sliney DH; American National Standards Institute. Maximum permissible exposures for ocular safety (ANSI 2000), with emphasis on ophthalmic devices. J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1250-65. doi: 10.1364/josaa.24.001250.
Results Reference
background
PubMed Identifier
15835362
Citation
Sliney D, Aron-Rosa D, DeLori F, Fankhauser F, Landry R, Mainster M, Marshall J, Rassow B, Stuck B, Trokel S, West TM, Wolffe M; International Commission on Non-Ionizing Radiation Protection. Adjustment of guidelines for exposure of the eye to optical radiation from ocular instruments: statement from a task group of the International Commission on Non-Ionizing Radiation Protection (ICNIRP). Appl Opt. 2005 Apr 10;44(11):2162-76. doi: 10.1364/ao.44.002162.
Results Reference
background
PubMed Identifier
15843671
Citation
Hansson GK. Inflammation, atherosclerosis, and coronary artery disease. N Engl J Med. 2005 Apr 21;352(16):1685-95. doi: 10.1056/NEJMra043430. No abstract available.
Results Reference
background
PubMed Identifier
22275207
Citation
Abramoff MD, Garvin MK, Sonka M. Retinal imaging and image analysis. IEEE Rev Biomed Eng. 2010;3:169-208. doi: 10.1109/RBME.2010.2084567.
Results Reference
background
PubMed Identifier
23322671
Citation
Tabatabaee A, Asharin MR, Dehghan MH, Pourbehi MR, Nasiri-Ahmadabadi M, Assadi M. Retinal vessel abnormalities predict coronary artery diseases. Perfusion. 2013 May;28(3):232-7. doi: 10.1177/0267659112473173. Epub 2013 Jan 15.
Results Reference
background
PubMed Identifier
11879113
Citation
Wong TY, Klein R, Sharrett AR, Duncan BB, Couper DJ, Tielsch JM, Klein BE, Hubbard LD. Retinal arteriolar narrowing and risk of coronary heart disease in men and women. The Atherosclerosis Risk in Communities Study. JAMA. 2002 Mar 6;287(9):1153-9. doi: 10.1001/jama.287.9.1153.
Results Reference
background
PubMed Identifier
23821191
Citation
Patel SR, Flanagan JG, Shahidi AM, Sylvestre JP, Hudson C. A prototype hyperspectral system with a tunable laser source for retinal vessel imaging. Invest Ophthalmol Vis Sci. 2013 Aug 1;54(8):5163-8. doi: 10.1167/iovs.13-12124.
Results Reference
background
PubMed Identifier
23791637
Citation
Shahidi AM, Patel SR, Flanagan JG, Hudson C. Regional variation in human retinal vessel oxygen saturation. Exp Eye Res. 2013 Aug;113:143-7. doi: 10.1016/j.exer.2013.06.001. Epub 2013 Jun 18.
Results Reference
background
PubMed Identifier
23518407
Citation
Kang MH, Balaratnasingam C, Yu PK, Morgan WH, McAllister IL, Cringle SJ, Yu DY. Alterations to vascular endothelium in the optic nerve head in patients with vascular comorbidities. Exp Eye Res. 2013 Jun;111:50-60. doi: 10.1016/j.exer.2013.03.005. Epub 2013 Mar 19.
Results Reference
background
PubMed Identifier
23538021
Citation
Koc S, Ozin B, Altin C, Altan Yaycioglu R, Aydinalp A, Muderrisoglu H. Evaluation of circulation disorder in coronary slow flow by fundus fluorescein angiography. Am J Cardiol. 2013 Jun 1;111(11):1552-6. doi: 10.1016/j.amjcard.2013.01.324. Epub 2013 Mar 25.
Results Reference
background
PubMed Identifier
25707042
Citation
Sayin N, Kara N, Uzun F, Akturk IF. A quantitative evaluation of the posterior segment of the eye using spectral-domain optical coherence tomography in carotid artery stenosis: a pilot study. Ophthalmic Surg Lasers Imaging Retina. 2015 Feb;46(2):180-5. doi: 10.3928/23258160-20150213-20.
Results Reference
background
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Evaluation of the Capacity of a Camera to Identify Signs of Arteriosclerosis in Retinal Arterioles
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