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Retinal scanning for biomarker discovery in multiple sclerosis

Multi-modal retinal scanning for diagnostic and therapeutic biomarker discovery in multiple sclerosis and neurodegenerative disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN77452114
Enrollment
100
Registered
2015-04-20
Start date
2015-04-01
Completion date
Unknown
Last updated
2016-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple sclerosis Nervous System Diseases Multiple sclerosis

Interventions

We will capture retinal images from consenting patients with MS and also healthy volunteers . We will identify candidate retinal biomarkers that could stratify MS patients, act as early indicators of

Sponsors

University of Edinburgh (UK)
Lead Sponsor
NHS Lothian (UK)
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Competent and consenting adults between the ages of 18 and 75 years 2. Patients with MS including those with clinically isolated syndrome, relapse-remitting, secondary progressive and primary progressive - 25 in each group 3. Participants must be able to manoeuvre themselves to the retinal imaging room in the Rowling Clinic unaided, sit upright in a chair or wheelchair, comfortably position themselves for imaging, and be able to listen to and act upon directions for fixing their gaze

Exclusion criteria

Exclusion criteria: 1. People who cannot manoeuvre themselves to the retinal imaging room in the Rowling Clinic unaided, who cannot sit upright in a chair or wheelchair, who cannot comfortably position themselves for imaging, or who would struggle with listening to or acting upon directions for fixing their gaze 2. People under the age 18 or over the age of 75

Design outcomes

Primary

MeasureTime frame
The change in retinal structure and function as measured by computation analysis of imaging.

Secondary

MeasureTime frame
Visual acuity (full contrast and reduced contrast), refractive error (from glasses or focimeter or refraction), and expanded disability status scale (EDSS). Correlation will be made with information on diagnosis, subtype, date of onset of symptoms, date of diagnosis, history of optic neuritis, history of other eye diseases, and any current visual symptoms. This will include phenotypic description, disease metric correlation, and integration of retinal image measurements into a combined score.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026