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NCT00762216 · ClinicalTrials.gov registry record · NA
Rotational Stability of the AcrySof® Toric
A NA study of Cataract, sponsored by Alcon Research.
- Completed
- Registry status
- NA
- Development phase
- 71
- Enrollment target
- 1
- Study location
NCT00762216: Completed NA study of Cataract, sponsored by Alcon Research.
NCT00762216 is a NA study of Cataract that has completed, run by Alcon Research. The registered enrollment target is 71 participants, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00762216, a NA study of Cataract, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- NA
- Development phase
- 71 participants
- Enrollment target
- 1
- Study location
Study Summary
To assess the rotational stability and the residual refractive cylinder and patient reported outcomes of the AcrySof Toric intraocular lens after unilateral or bilateral implantation.
Primary Outcome
Average magnitude of intraocular lens (IOL) rotation from day of surgery to 6-months post-surgery, measured in degrees.
Conditions Studied
Interventions
- DEVICE AcrySof® Toric intraocular lens
Study Locations (1)
Texas
- Alcon Call Center - Fort Worth
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 71 participants |
| Start Date | 2008-05 |
| Phase | NA |
What the finished NCT00762216 record still lists
NCT00762216 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (69% lower).
The record links to 1 condition, with Cataract appearing as the primary indexed condition, and to 1 intervention - of which AcrySof® Toric intraocular lens is the first listed.
NCT00762216 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT00762216 about?
NCT00762216 is a clinical study titled "Rotational Stability of the AcrySof® Toric". To assess the rotational stability and the residual refractive cylinder and patient reported outcomes of the AcrySof Toric intraocular lens after unilateral or bilateral implantation.
What is the current status of trial NCT00762216?
This trial is currently completed. It is a NA study. The enrollment target is 71 participants. The study started on 2008-05.
What conditions does trial NCT00762216 study?
This clinical trial studies the following conditions: Cataract.
What interventions are being tested in trial NCT00762216?
The interventions under investigation include: AcrySof® Toric intraocular lens (DEVICE).
Who is sponsoring clinical trial NCT00762216?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00762216 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT00762216's enrollment target sits among peer trials
71 47th of 83 higher than 37 of 83 other Cataract trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Cataract 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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