Assessment of Usefulness for Presbyopic Correction and Visual Function During Extended Depth of Field Contact Lens Wear.
Not Applicable
Recruiting
- Conditions
- presbyopia
- Registration Number
- JPRN-UMIN000051055
- Lead Sponsor
- MIYATA EYE HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Cases having ophthalmologic diseases such as severe dry eye, ocular inflammatory diseases, ocular infectous diseases, etc. Cases with a history of ophthalmic surgery. Cases who are judged to be ineligible for the study by the investigators
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual acuity at various distances
- Secondary Outcome Measures
Name Time Method functional visual acuity, contrast sensitivity, satisfaction (VAS scale), QOV (VFQ25, ATIONAL EYE INSTITUTE 42-ITEM REFRACTIVE ERROR QUALITY OF LIFE INSTRUMENT, accommodative microfluctuations
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie EDOF contact lens efficacy in presbyopic correction for JPRN-UMIN000051055?
How does EDOF lens performance in JPRN-UMIN000051055 compare to multifocal and monovision contact lenses for presbyopia?
Which biomarkers predict visual function improvement during EDOF contact lens wear in JPRN-UMIN000051055 presbyopia patients?
What adverse events are reported in JPRN-UMIN000051055 EDOF contact lens study and how are they managed?
Are alternative presbyopia correction methods like LASIK or progressive lenses more effective than EDOF in JPRN-UMIN000051055?