See if the Morrow eProgressive lenses work better than standard PALs for presbyopia
Official title: Evaluation of Functional Superiority of the Morrow eProgressive : A Comparative Study of Visual and Physical Comfort During Dynamic Activity
Run by Morrow Eyewear · NCT07878416 · Data updated 2026-11-12
This study tests whether the electronically adjustable Morrow eProgressive lenses help people with presbyopia see and move more naturally compared with traditional progressive lenses.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 45 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Morrow Eyewear Industry-sponsored |
| Locations | 3 sites (Antwerp and 2 other locations) |
| Status | Recruiting |
| Started | September 24, 2026 |
| Main results expected | February 28, 2027 |
| Study ends | February 28, 2027 |
| Registry record updated | October 16, 2026 |
| Trial ID | NCT07878416 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 45+ with presbyopia in both eyes, needing at least +1.75 add, suitable for Morrow glasses, and able to commit to the 2x3-week wearing schedule.
✕Probably not a fit
Individuals who do not adapt well to new eyewear or who have contraindicating ocular conditions may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Adults aged 45 and older with presbyopia will try both the Morrow eProgressive and standard PALs for three weeks each, in random order, across three sites in Belgium and Italy. The trial uses a randomized, open-label, crossover design so each participant serves as their own control. Researchers will measure eye and head movements during reading, assess stair descent performance, and collect visual comfort and lens preference data through questionnaires. The primary endpoint focuses on objective dynamic visual performance via eye-tracking metrics, with additional secondary outcomes including user-reported comfort and overall satisfaction.
Why it matters
Potential benefit: If successful, wearers may experience a larger usable visual field, more natural eye and head movements, and greater comfort with near tasks.
How similar studies have gone: Previous lens innovations in presbyopia have shown improved performance in some users, but this exact electronically adjustable approach is being evaluated prospectively in a crossover design.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged 45 or older, who are presbyopic in both eyes, with an inclusion criterium of minimum + 1.75 ADDition. * Suitable candidate for Morrow glasses * Willing and able to adhere to the study protocol and study procedures, and provide written consent prior to enrollment * Willing and able to strictly adhere to the 2 x 3-week spectacle-wearing schedule for all standard day-to-day activities, including a commitment to exclusive progressive wear of the assigned study spectacles (traditional PAL or Morrow eProgressive) throughout each respective study phase (temporary exceptions for sports or specific occasions are permitted using single-vision solutions only). * Current vision solution satisfaction below 8/10, as assessed by the study specific satisfaction questionnaire. Exclusion Criteria: * Individuals who do not yet require a reading addition for near tasks. * Distant BCVA worse than 20/25 (Snellen) or \>0.1 LogMar * Previous laser treatment for refractive correction. * Any previous refraction and/or intra-ocular surgery. * Any known systemic diseases affecting vision (e.g. diabetes, uncontrolled or unmedicated hypertension, autoimmune disease, inflammatory disease … ), at the discretion of the investigator * Associated strabismus (eyes not properly aligned) * Associated amblyopia (lazy eye) * Currently undergoing orthoptics therapy (exercises or treatments to fix eye movement problems or double vision) * Associated anisometropia \> 1.5 diopters
Where it's running
-
University Hospital Antwerp
Antwerp, Belgium Recruiting -
Meclinas
Mechelen, Belgium Not yet recruiting -
Research Centre in Optics & Optometry (COMiB), University of Milano Bicocca
Milan, Italy Not yet recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.