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Evaluation of subjective comfort and lens fit characteristics of daily disposable silicone hydrogel contact lenses (Precision 1) in first time contact lens wearing.

Evaluation of subjective comfort and lens fit characteristics of daily disposable silicone hydrogel contact lenses (Precision 1) in first time contact lens wearing. - Subjective comfort of daily disposable silicone hydrogel contact lenses in first time contact lens wearing.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000042265
Enrollment
50
Registered
2020-10-28
Start date
2020-10-26
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Myopia

Interventions

Sponsors

Teikyo University
Lead Sponsor
Nerima West Eye Clinic
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 13 to 40 years old must sign the informed consent. 2. Habitual eyeglasses wearers for vision correction and have never worn any contact lenses prior to enroll this clinical study. 3. Required lenses within the power range of study lenses to be fitted (-0.50D to -6.00D). 4. Vision correctable 0.8 (20/25) or better in each eye at distance with pre-study contact lenses at Baseline. 5. Have interest in wearing contact lenses as "very interested" or "fairly interested" and are willing to wear contact lenses for at least 8 hours per day and 5 days per week.

Exclusion criteria

Exclusion criteria: 1. Subjects with systemic diseases or ocular diseases, including dry eyes. 2. Subjects with a history of eye surgery/trauma local or systemic antibiotic or corticosteroid, immunomodulatory current medication, pregnancy or breastfeeding within 6 months of the enrollment visit. 3. Monocular subjects (only one eye with functional vision) or subjects fit with only one lens. 4. Participation in any clinical trial within 30 days of the enrollment visit. 5. Patient who in judged ineligible as patients in this clinical study by the investigator.

Design outcomes

Primary

MeasureTime frame
1)Corrective visual acuity 2)Lens centration/ fit 3)Subjective comfort 4)Subjective vision (QOV) 5)Convenience in wearing and removal of study lenses

Countries

Japan

Contacts

Public ContactTatsuya Mimura

Teikyo University School of Medicine, Department of Ophthalmology

mimurat@med.teikyo-u.ac.jp03-3964-1211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026