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NCT00721253 · ClinicalTrials.gov registry record · Phase 4
Visual Outcomes of Subjects Bilaterally Implanted With ReSTOR Aspheric +4 vs. Tecnis or Acri.LISA
A Phase 4 study, sponsored by Alcon Research.
- Completed
- Registry status
- Phase 4
- Development phase
- 42
- Enrollment target
NCT00721253 is a Phase 4 study that has completed, run by Alcon Research. The registered enrollment target is 42 participants.
The verdict
NCT00721253, a Phase 4 study, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 42 participants
- Enrollment target
Study Summary
This is a study to compare visual outcomes of subjects bilaterally implanted w/ReSTOR to subjects bilaterally implanted with the Tecnis Multifocal Intraocular Lens (IOL) or Acri.LISA IOL
Interventions
- DEVICE ReSTOR
- DEVICE Tecnis
- DEVICE Acri.LISA
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Start Date | 2007-07 |
| Est. Completion | 2008-10 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00721253
The ClinicalTrials.gov registry entry for NCT00721253 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 42 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which ReSTOR is the first listed.
NCT00721253 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00721253 about?
NCT00721253 is a clinical study titled "Visual Outcomes of Subjects Bilaterally Implanted With ReSTOR Aspheric +4 vs. Tecnis or Acri.LISA". This is a study to compare visual outcomes of subjects bilaterally implanted w/ReSTOR to subjects bilaterally implanted with the Tecnis Multifocal Intraocular Lens (IOL) or Acri.LISA IOL
What is the current status of trial NCT00721253?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 42 participants. The study started on 2007-07. Estimated completion is 2008-10.
What interventions are being tested in trial NCT00721253?
The interventions under investigation include: ReSTOR (DEVICE), Tecnis (DEVICE), Acri.LISA (DEVICE).
Who is sponsoring clinical trial NCT00721253?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
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