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NCT01249144 · ClinicalTrials.gov registry record · Phase 4
Visual and Refractive Outcomes After Implantation of Aspheric IOLs With Different Dioptric Increments and Manufacturing
A Phase 4 study, sponsored by Lenstec Incorporated.
- Terminated
- Registry status
- Phase 4
- Development phase
- 75
- Enrollment target
NCT01249144: Clinical Trial Phase 4 study, sponsored by Lenstec Incorporated.
NCT01249144 is a Phase 4 study that was terminated before completion, run by Lenstec Incorporated. The registered enrollment target is 75 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01249144, a Phase 4 study, was terminated before completion, sponsored by Lenstec Incorporated.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 75 participants
- Enrollment target
Study Summary
This study compares two intraocular lenses, the Softec HD and the Tecnis Z9002, used to replace the natural crystalline lens after cataract extraction. The variables compared include 1) the accuracy of targeted versus achieved refractive outcomes and 2) visual acuity outcomes three months after implantation.
Interventions
- DEVICE Intraocular Lens (IOL)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2010-10 |
| Est. Completion | 2012-01 |
| Phase | Phase 4 |
Why NCT01249144 stopped before completion
NCT01249144 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower).
The record links to 0 conditions, and to 1 intervention - of which Intraocular Lens (IOL) is the first listed.
NCT01249144 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01249144 about?
NCT01249144 is a clinical study titled "Visual and Refractive Outcomes After Implantation of Aspheric IOLs With Different Dioptric Increments and Manufacturing". This study compares two intraocular lenses, the Softec HD and the Tecnis Z9002, used to replace the natural crystalline lens after cataract extraction. The variables compared include 1) the accuracy of targeted versus achieved refractive outcomes and 2) visual acuity outcomes three months after impl...
What is the current status of trial NCT01249144?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 75 participants. The study started on 2010-10. Estimated completion is 2012-01.
What interventions are being tested in trial NCT01249144?
The interventions under investigation include: Intraocular Lens (IOL) (DEVICE).
Who is sponsoring clinical trial NCT01249144?
This trial is sponsored by Lenstec Incorporated, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01249144's enrollment target sits among peer trials
75 1002nd of 2000 higher than 974 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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