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Rod Sensitivity in Age-related Macular Degeneration (AMD) and Retinitis Pigmentosa (RP)

R

Retina Foundation of the Southwest

Status

Completed

Conditions

AMD
Retinitis Pigmentosa

Treatments

Diagnostic Test: Rod sensitivity

Study type

Observational

Funder types

Other

Identifiers

NCT03322930
STU082017-084

Details and patient eligibility

About

A new fundus-guided microperimeter (MP-3S) has been developed by Nidek, Inc. to track the fundus of the patient and present stimuli in specific anatomically-defined locations. Furthermore, this tracking means that exactly the same locations can be tested on subsequent (follow-up) visits. The investigators will use a method called two-color perimetry to map rod and cone sensitivity on this device. With this technique, the sensitivity difference (blue-red) to chromatic test stimuli can be used to determine whether rods, cones or both photoreceptor systems mediate the threshold at a given location in the macula.

Full description

Despite recent advances in understanding the pathogenesis of retinitis pigmentosa (RP) and age-related macular degeneration (AMD), precise characterization of the disease phenotype remains elusive. In both diseases, much of the focus has necessarily been on the loss of cone function, since visual fields, acuity and contrast sensitivity are typically measured under photopic conditions. In RP, we need a greater understanding of patterns of rod loss since most disease-causing mutations affect primarily rods. In AMD, recent findings have shown that scotopic sensitivity can be much more affected than conventional photopic measurements such as visual acuity. For patients, however, it is difficult to maintain stable fixation, especially when central vision is compromised. A new fundus-guided microperimeter, the MP-3S, has been developed by Nidek, Inc. to circumvent this problem. The investigators will evaluate the value of this device for following rod and cone loss in patients with either RP or AMD.

Enrollment

40 patients

Sex

All

Ages

10 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • clear media
  • diagnosis of RP or non neovascular AMD
  • normal volunteers

Exclusion criteria

  • exudative AMD
  • other eye diseases that could cause vision loss
  • physical ailments that would preclude comfortable testing
  • unable to provide informed consent

Trial design

40 participants in 2 patient groups

Retinitis Pigmentosa
Description:
patients with a diagnosis of retinitis pigmentosa and reduced rod function on baseline testing
Treatment:
Diagnostic Test: Rod sensitivity
Age-related Macular Degeneration
Description:
patients with a diagnosis of intermediate AMD and reduced rod function on baseline testing
Treatment:
Diagnostic Test: Rod sensitivity

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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