RecruitingNCT07582042

Lesion-tailored, Fundus-controlled Perimetry in Geographic Atrophy (GA).

Integration of Lesion-tailored, Fundus-controlled Perimetry Into Routine Clinical Care for Patients With Geographic Atrophy (GA) Receiving Pegcetacoplan Treatment in Accordance With the Approved Label.


Sponsor

University of Utah

Enrollment

50 participants

Start Date

Jun 15, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this observational study is to evaluate changes in retinal sensitivity over time in patients with geographic atrophy due to age related macular degeneration who are receiving pegcetacoplan as part of routine clinical care. The study aims to determine whether lesion tailored fundus-controlled perimetry can reliably measure functional changes near areas of atrophy and whether this testing can be implemented in everyday clinic care over 24 months. Participants will undergo repeated vision testing, standard eye imaging, and visual function questionnaires while continuing their prescribed treatment.


Eligibility

Min Age: 65 YearsMax Age: 90 Years

Inclusion Criteria9

  • Age 65-90 years.
  • Geographic Atrophy (GA) secondary to dry Age-related Macular Degeneration (AMD) in at least one eye with the following criteria:
  • GA lesion size between 1 and 15 mm² (≈ 0.4 to 6 disc areas)
  • GA borders must be at least 500 μm from the edge of the 30° × 25° optical coherence tomography (OCT) image frame
  • No confluent GA extending into peripapillary atrophy
  • Receiving intravitreal pegcetacoplan per label (at least one injection before screening).
  • Best-corrected visual acuity (BCVA) of 0.1 - 1.0 logMAR (≈ 20/20 to 20/200 Snellen)
  • Able to undergo mesopic FCP and required imaging.
  • Informed consent provided.

Exclusion Criteria5

  • Currently or previously active exudative macular neovascularization in the study eye.
  • High refractive errors (> ±5.00 Diopters \[D\] spherical equivalent) and significant astigmatism (> 2.50 D).
  • Ocular comorbidities likely to confound sensitivity or imaging (e.g., diabetic retinopathy with macular edema, retinal vein occlusion (RVO), inherited retinal disease, uncontrolled glaucoma).
  • Media opacity precluding reliable fundus-controlled perimetry (FCP) or imaging (e.g., dense cataract, corneal opacity, vitreous hemorrhage).
  • Any systemic condition judged likely to compromise participation, follow-up, or data integrity.

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Locations(1)

University of Utah, Department of Ophthalmology, John A. Moran Eye Center

Salt Lake City, Utah, United States

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NCT07582042


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