Deciphering AMD by Deep Phenotyping and Machine Learning- Prospective Study - PINNACLE
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- STATUS
- Recruiting
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- participants needed
- 400
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- sponsor
- University of Southampton
Summary
We will conduct a prospective non-interventional study including 400 early AMD patients (=600 untreated early AMD eyes, including both unilateral (AREDS IV) and bilateral (AREDS II)) over 3 years to specifically investigate the morphological sequence of events preceding the conversion towards late AMD. All patients will be followed by OCT imaging every 4 months to detect the earliest focal sites of disease progression. As soon as focal areas of change are observed by the VRC, a targeted follow-up schedule will be triggered to investigate the events at that area of change in a targeted manner.
Description
We will recruit patients with 1) intermediate AMD in one eye and advanced AMD in the non-study eye or 2) patients with bilateral intermediate AMD (where both eyes will be included). As some participants are symptomless at the stage of intermediate AMD, we will recruit from hospital databases including imaging databases and ophthalmology and optometry practices and engagement with Patient Societies e.g. the Macular Society and patient public involvement meetings.
There will be four clinical sites performing detailed assessments on 50 patients each and, to
increase sample size, an additional eight referral sites in the UK who will each enrol and
follow 25 study patients by
After consent, patients will undergo visual function tests (ETDRS visual acuity,
microperimetry) and multimodal imaging including fundus photographs, OCT scans, OCT
200 patients (main cohort) will undergo dense
Details
Condition | age-related macular degeneration |
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Age | 55years - 90years |
Clinical Study Identifier | NCT04269304 |
Sponsor | University of Southampton |
Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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