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NCT00425464 · ClinicalTrials.gov registry record · Phase 3
A Prospective Multicenter Clinical Study to Evaluate the Safety and Effectiveness of the Synchrony Dual Optic Intraocular Lens in Patients Undergoing Cataract Extraction
A Phase 3 study, sponsored by Abbott Medical Optics.
- Terminated
- Registry status
- Phase 3
- Development phase
- 410
- Enrollment target
NCT00425464 is a Phase 3 study that was terminated before completion, run by Abbott Medical Optics. The registered enrollment target is 410 participants.
The verdict
NCT00425464, a Phase 3 study, was terminated before completion, sponsored by Abbott Medical Optics.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 410 participants
- Enrollment target
Study Summary
The purpose of the study is to determine if the Synchrony Dual Optic Accommodating Intraocular Lens can be used safely and effectively in post cataract extraction subjects
Interventions
- DEVICE Standard Monofocal Intraocular Lens
- DEVICE Synchrony® Dual Optic Intraocular Lens
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 410 participants |
| Start Date | 2005-11 |
| Est. Completion | 2013-04 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00425464
The ClinicalTrials.gov registry entry for NCT00425464 describes a study currently listed as terminated, categorized as Phase 3. The registered enrollment target is 410 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Optics, which has 14 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Standard Monofocal Intraocular Lens is the first listed.
NCT00425464 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00425464 about?
NCT00425464 is a clinical study titled "A Prospective Multicenter Clinical Study to Evaluate the Safety and Effectiveness of the Synchrony Dual Optic Intraocular Lens in Patients Undergoing Cataract Extraction". The purpose of the study is to determine if the Synchrony Dual Optic Accommodating Intraocular Lens can be used safely and effectively in post cataract extraction subjects
What is the current status of trial NCT00425464?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 410 participants. The study started on 2005-11. Estimated completion is 2013-04.
What interventions are being tested in trial NCT00425464?
The interventions under investigation include: Standard Monofocal Intraocular Lens (DEVICE), Synchrony® Dual Optic Intraocular Lens (DEVICE).
Who is sponsoring clinical trial NCT00425464?
This trial is sponsored by Abbott Medical Optics, which has 14 total clinical trials registered on ClinicalTrials.gov.
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