Status:

ENROLLING_BY_INVITATION

Microperimetry Changes in Retinal Function in Macular Disorders

Lead Sponsor:

University of Nottingham

Conditions:

Dry AMD

Diabetic Retinopathy (DR)

Eligibility:

All Genders

21+ years

Brief Summary

The purpose of this study is to measure precisely how sensitive the central part of the retina - the light-sensitive film at the back of the eye, is to light. We will use a special device called the M...

Eligibility Criteria

Inclusion

  • A. Patients
  • Inclusion Criteria:
  • Adult age above 21 years old.
  • Signed informed consent
  • Visual acuity Log MAR 0.0 to 1.2
  • Patients diagnosed with:
  • Geographic atrophy (AMD).
  • Diabetic without retinopathy, and minimal to moderate non-proliferative diabetic retinopathy (NPDR) with or without presence of macular oedema on optical coherence tomography (OCT)
  • Control group of age matched participants without any retinal disease, glaucoma or optic nerve disease in either eye Patients willing to attend follow-up MP examinations. (This does not apply to normal controls who only require one attendance).
  • Exclusion Criteria
  • Moderate to severe cataract (over grade 2) or other cause of opaque optical media that will preclude adequate fundoscopy or MP assessment.
  • Previous treatments in the eye with intravitreal therapies of anti-VEGFs or steroids within the previous 6 months, or macular laser photocoagulation
  • Active vascular event in either eye any examination time.
  • Participants who are unable/unwilling to provide consent
  • Participants who are unable to read English fluently
  • B. Normal Controls Inclusion Criteria
  • Normal controls will include persons who are not diabetic, and do not have glaucoma, any retinal or optic nerve disease.
  • Signed informed consent
  • Adult age above 21 years old. No upper age limit.
  • Visual acuity LogMAR \<0.2.
  • Controls should be willing to attend once only.
  • Exclusion criteria
  • Moderate to severe cataract (over grade 2) or other cause of opaque optical media
  • Previous treatments in the particular eye with intravitreal therapies of anti-VEGFs or steroids within the previous 6 months, or macular laser photocoagulation
  • Active/previous vascular event in either eye e.g. retinal arterial or vein occlusion, ischaemic optic neuropathy, or glaucoma
  • Persons with diabetes
  • Participants who are unable to read English fluently
  • Participants who are unable/unwilling to provide consent

Exclusion

    Key Trial Info

    Start Date :

    April 4 2025

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    August 30 2026

    Estimated Enrollment :

    200 Patients enrolled

    Trial Details

    Trial ID

    NCT07170683

    Start Date

    April 4 2025

    End Date

    August 30 2026

    Last Update

    September 12 2025

    Active Locations (1)

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    1

    Nottingham University Hospitals NHS Trust

    Nottingham, Notts, United Kingdom, NG7 2UH