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NCT00720005 · ClinicalTrials.gov registry record
Evaluation of the Aspheric ReSTOR IOL After Routine Cataract Extraction
A clinical trial of Cataract, sponsored by Medical University of South Carolina.
- Completed
- Registry status
- 20
- Enrollment target
- 1
- Study location
NCT00720005: Completed study of Cataract, sponsored by Medical University of South Carolina.
NCT00720005 is a study of Cataract that has completed, run by Medical University of South Carolina. The registered enrollment target is 20 participants, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00720005, a study of Cataract, has completed, sponsored by Medical University of South Carolina.
- COMPLETED
- Registry status
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to evaluate the visual outcomes and patient satisfaction after bilateral implantation of the aspheric ReSTOR multifocal intraocular lens (IOL) and compare it to a historical control group of patients implanted bilaterally with the spherical ReSTOR multifocal
Conditions Studied
Interventions
- DEVICE Aspheric Acrysof ReSTOR intraocular lens
Study Locations (1)
South Carolina
- Storm Eye Institute, Medical University of South Carolina - Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2007-09 |
| Est. Completion | 2008-12 |
What the finished NCT00720005 record still lists
NCT00720005 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (91% lower).
The record links to 1 condition, with Cataract appearing as the primary indexed condition, and to 1 intervention - of which Aspheric Acrysof ReSTOR intraocular lens is the first listed.
NCT00720005 reports a single indexed study location in South Carolina.
Frequently Asked Questions
What is clinical trial NCT00720005 about?
NCT00720005 is a clinical study titled "Evaluation of the Aspheric ReSTOR IOL After Routine Cataract Extraction". The purpose of this study is to evaluate the visual outcomes and patient satisfaction after bilateral implantation of the aspheric ReSTOR multifocal intraocular lens (IOL) and compare it to a historical control group of patients implanted bilaterally with the spherical ReSTOR multifocal
What is the current status of trial NCT00720005?
This trial is currently completed. The enrollment target is 20 participants. The study started on 2007-09. Estimated completion is 2008-12.
What conditions does trial NCT00720005 study?
This clinical trial studies the following conditions: Cataract.
What interventions are being tested in trial NCT00720005?
The interventions under investigation include: Aspheric Acrysof ReSTOR intraocular lens (DEVICE).
Who is sponsoring clinical trial NCT00720005?
This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00720005 being conducted?
This trial has 1 study location across South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT00720005's enrollment target sits among peer trials
20 79th of 83 higher than 2 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.
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