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NCT00625313 · ClinicalTrials.gov registry record · NA
Clinical Study of a UV-Absorbing Acrylic Posterior Chamber Intraocular Lens
A NA study, sponsored by Hoya Surgical Optics.
- Completed
- Registry status
- NA
- Development phase
- 617
- Enrollment target
NCT00625313: Completed NA study, sponsored by Hoya Surgical Optics.
NCT00625313 is a NA study that has completed, run by Hoya Surgical Optics. The registered enrollment target is 617 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (56% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00625313, a NA study, has completed, sponsored by Hoya Surgical Optics.
- COMPLETED
- Registry status
- NA
- Development phase
- 617 participants
- Enrollment target
Study Summary
The purpose of this study is to assess the safety and efficacy of the HMY Model YA-60BB Intraocular Lens (IOL) when implanted in the posterior chamber of the human eye for the optical correction of aphakia following cataract extraction.
Interventions
- DEVICE HMY Model YA-60BB IOL
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 617 participants |
| Start Date | 2004-03 |
| Est. Completion | 2008-12 |
| Phase | NA |
What the finished NCT00625313 record still lists
NCT00625313 is an interventional study that assigns participants to a tested intervention. The registered 617 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (56% lower).
The record links to 0 conditions, and to 1 intervention - of which HMY Model YA-60BB IOL is the first listed.
NCT00625313 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00625313 about?
NCT00625313 is a clinical study titled "Clinical Study of a UV-Absorbing Acrylic Posterior Chamber Intraocular Lens". The purpose of this study is to assess the safety and efficacy of the HMY Model YA-60BB Intraocular Lens (IOL) when implanted in the posterior chamber of the human eye for the optical correction of aphakia following cataract extraction.
What is the current status of trial NCT00625313?
This trial is currently completed. It is a NA study. The enrollment target is 617 participants. The study started on 2004-03. Estimated completion is 2008-12.
What interventions are being tested in trial NCT00625313?
The interventions under investigation include: HMY Model YA-60BB IOL (DEVICE).
Who is sponsoring clinical trial NCT00625313?
This trial is sponsored by Hoya Surgical Optics, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00625313's enrollment target sits among peer trials
617 161st of 2000 higher than 1,840 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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