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| Name | Class |
|---|---|
| Aston University | OTHER |
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A study to assess the utility of human polarization pattern perception for the detection, diagnosis and monitoring of eye disease
The recently described high sensitivity of the human eye to differentiate small angular differences in linear polarization and evidence supporting its macular origin (Misson, Anderson; 2017) suggests that human polarization sensitivity might be a useful diagnostic tool for macular disease. This augments a previous study in which we demonstrated the ability of the human visual system to detect isochromatic isoluminant polarization modulated pattern stimuli (Misson et al 2015).
This is an exploratory 'proof-of-concept' study to determine the clinical value of polarization pattern perception, PPP, in health and disease. We further propose that PPP might be valuable for the diagnosis, monitoring and early detection of macular disease. The latter includes common blinding conditions such as age related macular degeneration and diabetic retinopathy. It is also intended to investigate the effect of cataracts and cataract surgery on PPP: cataract surgery modifies the optics of the eye so might also modify PPP.
PPP is measured using a modification of the methodology described in (Misson et al 2015) and (Misson, Anderson; 2017) whereby polarization modulated patterns are presented on a modified LCD display. The observer's task is to report if they see an image and to describe the image. Images comprise simple patterns or traditional optotypes. A standard set of images are presented in pseudorandom order and the response recorded. A total score, the polarization pattern perception score PPP is then determined from the number of images seen/identified. A more refined metric, the polarization visual acuity pVA, will be derived from the response to the optotype stimuli. These data are then compared to conventional tests of visual structure and function including logMAR visual acuity, ocular examination and OCT scan data.
The study in anticipated to comprise:
Phase 1. Normative Evaluation: observational prospective cross-sectional.. A preliminary normative study will be undertaken on staff members. The aim is to quantify normative values in preparation for the clinical studies.
Hypotheses to be tested:
Phase 2 Patient Group: observational Prospective cross-sectional / case-control.
Phase 2 subjects will comprise normals and patients with cataracts/pseudophakia and/or AMD, other macular pathology, diabetic retinopathy..
The aim of this phase is to determine the effect, if any, of particular eye conditions on pVA/PPP alone and in comparison with other test parameters.
Hypotheses to be tested:
Phase 3: Cataract pre-op v post op pVA/PPP: prospective interventional case-control.
Timescale:concurrent with Phase 2 A subset of the phase 2 cataract patients will undergo cataract surgery according to clinical need. These patients are routinely reviewed 4 - 8 weeks post-op when the opportunity will arise to repeat pVA/PPP measurement. The fellow eye will serve as a control / provide data for repeatability assessment.
The aims of this phase are
Hypotheses:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Normal | phakic participants with no evidence of eye disorders |
| |
| Cataract | participants with cataract |
| |
| AMD | participants with age related macular degeneration |
| |
| Pseudophakic | particpiants who have had cataract surgery with intraocular lens implant |
| |
| other macula | participants with macular ddisorders other than AMD |
| |
| DR | participants with diabetic retinopathy |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| polarization sensitivity | Diagnostic Test | test of polarization vision as described in Study Description |
|
| Measure | Description | Time Frame |
|---|---|---|
| polarization sensitivity | determine and compare polarization sensitivity between groups | 18 month |
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Inclusion Criteria:
- willing and able to provide informed consent
Exclusion Criteria:
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Patients and staff of the Eye Department of South Warwickshire NHS Trust
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Gary P Misson, PhD FRCOphth | Contact | +44 01926495321 | gary.misson@swft.nhs.uk | |
| Jo Williams | Contact | +44 01926495321 | jo.williams@swft.nhs.uk |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| South Warwickshire NHS Foundation Trust | Recruiting | Warwick | Warwickshire | CV37 0PZ | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 26291073 | Result | Misson GP, Timmerman BH, Bryanston-Cross PJ. Human perception of visual stimuli modulated by direction of linear polarization. Vision Res. 2015 Oct;115(Pt A):48-57. doi: 10.1016/j.visres.2015.08.004. Epub 2015 Aug 28. | |
| 29185499 | Result | Misson GP, Anderson SJ. The spectral, spatial and contrast sensitivity of human polarization pattern perception. Sci Rep. 2017 Nov 29;7(1):16571. doi: 10.1038/s41598-017-16873-6. |
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| ID | Term |
|---|---|
| D002386 | Cataract |
| D008268 | Macular Degeneration |
| D019591 | Pseudophakia |
| D003930 | Diabetic Retinopathy |
| D012164 | Retinal Diseases |
| ID | Term |
|---|---|
| D007905 | Lens Diseases |
| D005128 | Eye Diseases |
| D012162 | Retinal Degeneration |
| D012816 | Signs and Symptoms |
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| D013568 |
| Pathological Conditions, Signs and Symptoms |
| D003925 | Diabetic Angiopathies |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D048909 | Diabetes Complications |
| D003920 | Diabetes Mellitus |
| D004700 | Endocrine System Diseases |