Optimized MP MVA refractive technique for better visual performance

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, multicenter, non-interventional observational study that compares visual outcomes between two sites while masking examiners. It includes patients previously enrolled in Hoya studies or previously implanted with non-toric monofocal IOLs, focusing on distance-corrected intermediate visual acuity. The study aims to demonstrate non-inferiority of mean DCIVA between Site 1 and Site 2. Participation does not involve an active treatment, and data are collected from existing IOL recipients during routine follow-up visits. The design supports exploratory sub-analysis for eyes with specific prior IOL histories.

Why it matters

Who can join: the full rules

Inclusion Criteria:

Main study:

1. Previously implanted with intraocular lens through 2 previous IOL studies;
2. Clear intraocular media with no clinically significant opacity, in the investigator's judgment, that would affect visual acuity;
3. Able to provide informed consent and complete all required study procedures.

Exploratory sub-study:

1\. Additional inclusion criteria: Pseudophakic eyes implanted with one of the IOLs in one eye from 3 previous IOL studies

Exclusion Criteria:

Main study:

1. Corrected distance visual acuity (CDVA) worse than 0.2 logMAR (or 20/32 Snellen)
2. Subjects with ongoing medical conditions or treatment that might impact outcomes during the study visit as determined by the investigator.

Exploratory sub-study:

1\. Additional exclusion criteria: Pseudophakic eyes with oblique residual astigmatism.

Where it's running

• Peregrine Eye Laser Institute
  Manila, Philippines Recruiting

Study contacts

• Study coordinator: Srividhya Medical Monitor
• Email: srividhya.vilupuru@hoya.com
• Phone: +1-909-680-3900

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.