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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 is a Phase 4 study that was terminated before completion, run by Lenstec Incorporated. The registered enrollment target is 75 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01249144
The ClinicalTrials.gov registry entry for NCT01249144 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Lenstec Incorporated, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Intraocular Lens (IOL) is the first listed.
NCT01249144 reports 0 study locations.
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.
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