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Not yet recruitingNCT07171541Updated Sep 12, 2025

Correlation Between OCT and Mf-ERG Findings With BCVA in Patients With Macular Dystrophy

An observational study in Macular Dystrophy, sponsored by New Valley University. Not yet recruiting. Per ClinicalTrials.gov, last updated 2025-09-12.

Sponsored by New Valley University · Observational

From the registry’s dates

  • Primary completion was expected by Nov 2025, 10 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
30
Sex
All
01

Study summary

Correlation between optical coherence tomography and multifocal electroretinogram findings with visual acuity in patients with macular dystrophy.

Read the detailed description

Macular dystrophies cause progressive central vision loss, but the relationship between structural retinal changes (OCT) and functional deficits (mf-ERG) with visual outcomes remains poorly understood. Current clinical assessment relies primarily on visual acuity, which inadequately reflects retinal damage or predicts disease progression. This knowledge gap limits prognostic accuracy and optimal patient management. Recent advances in OCT and mf-ERG technology provide an opportunity to establish robust structure-function correlations. Understanding these relationships will enhance patient care through improved prognosis, standardized monitoring protocols, and better clinical trial outcome measures for macular dystrophy patients.

02

Conditions studied

  • Macular Dystrophy
03

In context

Macular Degeneration

1,474 studies on the registry are indexed under Macular Degeneration; 206 are open to participants now.

This study's planned enrollment of 30 is below the median of 106 across 421 observational studies indexed under Macular Degeneration.

Browse Macular Degeneration studies →

Lead sponsor

New Valley University is the lead sponsor of 23 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

All patients diagnosed with macular dystrophy during the period of the study

Inclusion criteria

  • All patients diagnosed with macular dystrophy in Tiba Eye Centre, Egypt, Assiut, during the period of the study

Exclusion criteria

Exclusion Criteria:

  • The patients diagnosed with macular dystrophy refuse to contribute to the study.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testOCT ,mFERG,VA test

    retinal photography by OCT, VA measurement, and mfERG test

06

What researchers measure

Primary outcomes

  1. BCVA (best corrected visual acuity)

    BCVA was recorded in 30 eyes of 30 patients with macular dystrophy.

    Time frame: Day 1/month 3

  2. CMT (central macular thickness) μm Central macular thickness measurement using optical coherence tomography

    CMT (central macular thickness) in μm in 30 eyes of 30 patients with macular dystrophy Central macular thickness measurement using optical coherence tomography.

    Time frame: Day1/month 3

  3. mf-ERG amplituide nV/deg2

    mf-ERG amplitude nV/deg² in 30 eyes of 30 patients with macular dystrophy multifocal electroretinogram amplitude measurement using the mf-ERG machine

    Time frame: Day 1/month 6

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 12, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07171541
Lead sponsor
New Valley University
Collaborators
Assiut University
Responsible party
Asmaa Kamel Ahmed Hassan (Dr.principle investigators/ Lecture of ophthalmology ,faculty of medicine , New Valley University, New Valley University) — Principal investigator
First posted
Sep 12, 2025
Start date
Sep 20, 2025 (estimated)
Primary completion
Nov 20, 2025 (estimated)
Completion
Dec 20, 2025 (estimated)
Last update
Sep 12, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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