Colour Contrast Sensitivity for the Early Detection of Wet Age-related Macular Degereration (CEDAR)
Avainsanat
Abstrakti
Kuvaus
Neovascular age‐related macular degeneration (nARMD), which by definition affects the over 50s, accounts for more than 50% of visual impairment certifications in the United Kingdom1 and a recent study2 estimates the prevalence in the UK at 1.2% in individuals aged 50 or more, 2.5% in those over 65, and 6.3% in those aged 80 or more. Neovascular ARMD is therefore likely to become a much more significant issue as the population ages, unless steps are taken now to find ways of limiting loss of vision: the same study2 suggests there are currently 263,000 cases of nARMD in the UK, but the number is set to increase by almost a third by the year 2020. Importantly, individuals with poor vision also have a higher frequency of falls and of depression compared to aged‐matched people with normal vision, and are likely to live alone and have additional health problems3, 4. Therefore nARMD significantly impacts on quality of life, to a much greater extent than appreciated by many health professionals: a key study5 reported that even mild sight impairment results in a 17% decrease in quality of life, whereas moderate and severe sight impairment result in a 40% and 63% decrease in quality of life respectively. It should be noted that a 63% decrease in quality of life is comparable to that encountered with advanced prostatic cancer with uncontrollable pain or a severe stroke that leaves a person bedridden, incontinent and requiring constant nursing care5.
The advent of anti‐VEGF therapy in nARMD and the approval of ranibizumab (Lucentis) in the UK by the National Institute for Clinical Excellence (NICE) has dramatically improved the prognosis of patients with nARMD: vision can frequently be maintained or even improved, particularly if early detection and treatment occur6‐9. However it is currently difficult to detect and monitor nARMD in its early stages and most individuals typically present to the ophthalmologist only once a certain degree of irreversible damage has occurred. The hallmark of nARMD is a choroidal neovascular membrane (CNV) 1, 10, 11, although changes occur locally before a CNV develops, as follows:
1. Inflammatory mediators are released in the affected area and changes in metabolism develop12‐15.
2. The retina affected by the insult gradually loses its function10‐12, 14‐18. It has yet to be established at which point of CNV development the surrounding retina has detectable functional and structural abnormalities, however a wealth of literature10‐12, 14‐19 suggests it starts when the patient is still asymptomatic and before currently available non‐invasive imaging techniques are able to detect any abnormality. Many studies10, 12, 17, 18, 20 indicate that the above mentioned changes in metabolism determine abnormal function in the overlying photoreceptors/inner retina very early in the disease process, with some cone populations affected more than others18, 20, 21. The same studies suggest it is possible to detect this localised abnormal retinal function early with colour contrast sensitivity (CCS), especially in the blue‐yellow (tritan) axis. The investigators therefore propose this technique can be utilised to identify people at risk of developing nARMD and those with the early, presymptomatic stage of the disease. The study will also evaluate other modalities which test either structure or function of the retina, to establish if any can be used for the early detection of nARMD.
Päivämäärät
Viimeksi vahvistettu: | 12/31/2018 |
Ensimmäinen lähetys: | 03/19/2014 |
Arvioitu ilmoittautuminen lähetetty: | 06/23/2014 |
Ensimmäinen lähetetty: | 06/24/2014 |
Viimeisin päivitys lähetetty: | 01/08/2019 |
Viimeisin päivitys lähetetty: | 01/09/2019 |
Todellinen opintojen alkamispäivä: | 09/30/2014 |
Arvioitu ensisijainen valmistumispäivä: | 04/30/2017 |
Arvioitu tutkimuksen valmistumispäivä: | 04/30/2017 |
Ehto tai tauti
Interventio / hoito
Other: Colour contrast sensitivity
Vaihe
Varren ryhmät
Varsi | Interventio / hoito |
---|---|
Colour contrast sensitivity Colour contrast sensitivity | Other: Colour contrast sensitivity Reading of numbers or letters from a monitor |
Kelpoisuusehdot
Tutkimukseen soveltuvat iät | 50 Years Vastaanottaja 50 Years |
Sukupuolet, jotka ovat kelpoisia tutkimukseen | All |
Näytteenottomenetelmä | Non-Probability Sample |
Hyväksyy terveelliset vapaaehtoiset | Joo |
Kriteeri | Inclusion Criteria: - Over 50 years of age - Unilateral wet ARMD Exclusion Criteria: - Bilateral wet ARMD - Other retinal pathology - High refractive error - Not fluent in English - Unable to give informed consent |
Tulokset
Ensisijaiset tulosmittaukset
1. Capability of evaluated techniques detecting asymptomatic wet ARMD [24 months]
Toissijaiset tulosmittaukset
1. Improve understanding of the disease process in wet ARMD [24 months]