Actively Recruiting

Age: 7Years +
All Genders
Healthy Volunteers
ID01866371

High Resolution Retinal Imaging

Led by University of Pennsylvania · Updated on 2026-05-05

600

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

N

National Eye Institute (NEI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying the detailed structure and function of the normal and diseased retina to improve detection, diagnosis, and treatment of retinal diseases like Stargardts, Retinitis Pigmentosa, Age-related Macular Degeneration, Choroideremia, and Geographic Atrophy. The study uses a special imaging tool called an adaptive optics scanning laser ophthalmoscope (AOSLO) to capture high-resolution images of the retina at a cellular level. The main goal is to compare these images between people with and without retinal diseases by examining cell density, size, spacing, and the arrangement of the cone photoreceptor mosaic and other retinal layers. Participants include two groups: one with retinal degeneration and vision abnormalities, and a control group without these conditions. Both groups undergo retinal imaging procedures such as adaptive optics imaging, optical coherence tomography, and fundus photography. Vision tests including microperimetry, visual fields, and visual acuity assessments are also performed. The study mainly involves an initial visit lasting one day for these imaging and vision assessments. During their participation, subjects will have their retina imaged with the AOSLO and other imaging methods to produce detailed pictures of retinal cells and layers. Researchers will analyze these images to study differences in retinal structure. Measurements like cone mosaic parameters are taken during the initial visit. The study allows for long-term follow-up with participants aged 7 and older to understand retinal changes over time. All procedures are non-invasive and carefully monitored by study personnel.

CONDITIONS

Brief Title

High Resolution Retinal Imaging

Who Can Participate

Age: 7Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Males or females age 7 years or older.
  • Parental or guardian permission (informed consent) and, if appropriate, child assent for ages 7 to 17.
  • Ability to reasonably comply with the imaging protocol as determined by study staff.
Not Eligible

You will not qualify if you...

  • Individuals at risk for acute glaucoma.
  • Individuals who are photophobic and have adverse psychological reactions to flashes of light.
  • Presence of ocular opacities, high refractive error, or frequent nystagmus as determined by the study team.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo retinal imaging procedures including adaptive optics imaging, optical coherence tomography, and fundus photography. Vision may also be assessed using microperimetry, visual fields, and visual acuity.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 10 years

Participants are observed over time to monitor retinal health and vision changes without active treatment.

Visit schedule depends on participant group and study protocol

Trial Site Locations

Total: 1 location

1

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

J

Jessica IW Morgan, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial