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The Effect of the Free-toroidal Design Lenses on the Subjective Visual Quality in the Myopic Population

The Effect of the Free-toroidal Design Lenses on the Subjective Visual Quality in the Myopic Population

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05684302
Enrollment
200
Registered
2023-01-13
Start date
2021-01-01
Completion date
2021-12-24
Last updated
2023-01-13

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

Conditions

Myopia, Refractive Errors

Brief summary

A prospective, self-control, double-blind design was conducted in Tianjin. Two hundred participants were assigned to wear two kinds of spectacle glasses. To examine the effect of free-toroidal design and aspherical lens on the subjective visual quality among the myopic population.

Detailed description

A prospective, self-control, double-blind design was conducted in Tianjin. Two hundred participants were assigned to wear two kinds of spectacle glasses. To examine the effect of free-toroidal design and aspherical lens on the subjective visual quality among the myopic population. The subjective visual quality of clarity and comfort were determined using a questionnaire when first wearing the glasses and after 1week.

Interventions

OTHERThe free-toroidal design lenses

Participants were asked to wear the new design lenses (the free-toroidal design lenses) for 1 week

Sponsors

Tianjin Eye Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years

Inclusion criteria

* health volunteers * their spherical refraction from -0.50 to -8.00 Diopter, with the cylinder diopter less than -3.00 Diopter * best corrected visual acuity (BCVA)≥ 20/20 in both eyes * stable refraction (no change greater than 0.5 Diopter within two years)

Exclusion criteria

* if they had Aphakic or intraocular lens eyes, had a history of trauma, active eye disease or ocular surgery, serious systemic diseases, or had a wearing history of corneal contact lenses.

Design outcomes

Primary

MeasureTime frameDescription
The clarity scorebaseline visit timeThe clarity score by a questionnaire,scores on the questionnaire range from 1 to 6, with higher scores being better
The comfort scorebaseline visit timeThe comfort score by a questionnaire,scores on the questionnaire range from 1 to 6, with higher scores being better

Secondary

MeasureTime frameDescription
Accuracy of foveal and peripheral visual acuitybaseline visit timeAccuracy of foveal and peripheral visual acuity was assessed by the eye movement tracking device

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026