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NCT01061918 · ClinicalTrials.gov registry record · Phase 4
Evaluation Of Bilateral Tecnis Multifocal Versus ReSTOR 3D Intraocular Lenses
A Phase 4 study, sponsored by Innovative Medical.
- Completed
- Registry status
- Phase 4
- Development phase
- 40
- Enrollment target
NCT01061918: Completed Phase 4 study, sponsored by Innovative Medical.
NCT01061918 is a Phase 4 study that has completed, run by Innovative Medical. The registered enrollment target is 40 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01061918, a Phase 4 study, has completed, sponsored by Innovative Medical.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 40 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the visual outcomes with bilateral implantation of Tecnis MF and ReSTOR intraocular lenses (IOLs) 6 months post cataract surgery.
Interventions
- DEVICE ReSTOR
- DEVICE Tecnis MF
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2009-08 |
| Est. Completion | 2010-12 |
| Phase | Phase 4 |
What the finished NCT01061918 record still lists
NCT01061918 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 2 interventions - of which ReSTOR is the first listed.
NCT01061918 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01061918 about?
NCT01061918 is a clinical study titled "Evaluation Of Bilateral Tecnis Multifocal Versus ReSTOR 3D Intraocular Lenses". The purpose of this study is to compare the visual outcomes with bilateral implantation of Tecnis MF and ReSTOR intraocular lenses (IOLs) 6 months post cataract surgery.
What is the current status of trial NCT01061918?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2009-08. Estimated completion is 2010-12.
What interventions are being tested in trial NCT01061918?
The interventions under investigation include: ReSTOR (DEVICE), Tecnis MF (DEVICE).
Who is sponsoring clinical trial NCT01061918?
This trial is sponsored by Innovative Medical, which has 44 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01061918's enrollment target sits among peer trials
40 1397th of 2000 higher than 533 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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