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NCT00759096 · ClinicalTrials.gov registry record · NA
Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL
A NA study of Visual Acuity, sponsored by Alcon Research.
- Completed
- Registry status
- NA
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT00759096 is a NA study of Visual Acuity that has completed, run by Alcon Research. The registered enrollment target is 30 participants, below the 139-participant average among 20 other Visual Acuity trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00759096, a NA study of Visual Acuity, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to assess uniocular and binocular unaided distance, intermediate, and near VA; contrast sensitivity, accommodation amplitude, stereopsis, glare testing, ocular aberrations and the clinical satisfaction assessment after bilateral implant of the Restor IOL.
Conditions Studied
Interventions
- DEVICE RESTOR IOL Model SA60D3
Study Locations (1)
Texas
- Alcon Call Center - Fort Worth
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2007-05 |
| Est. Completion | 2008-07 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00759096
The ClinicalTrials.gov registry entry for NCT00759096 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 139-participant average among 20 other Visual Acuity trials with a reported enrollment target (78% lower). The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Visual Acuity appearing as the primary indexed condition, and to 1 intervention - of which RESTOR IOL Model SA60D3 is the first listed.
NCT00759096 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT00759096 about?
NCT00759096 is a clinical study titled "Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL". The purpose of this study is to assess uniocular and binocular unaided distance, intermediate, and near VA; contrast sensitivity, accommodation amplitude, stereopsis, glare testing, ocular aberrations and the clinical satisfaction assessment after bilateral implant of the Restor IOL.
What is the current status of trial NCT00759096?
This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2007-05. Estimated completion is 2008-07.
What conditions does trial NCT00759096 study?
This clinical trial studies the following conditions: Visual Acuity.
What interventions are being tested in trial NCT00759096?
The interventions under investigation include: RESTOR IOL Model SA60D3 (DEVICE).
Who is sponsoring clinical trial NCT00759096?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00759096 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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