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NCT00759668 · ClinicalTrials.gov registry record · NA
Visual Function and Patient Satisfaction After Bilateral Implantation of AcrySof Natural ReSTOR (Model SN60D3) or AcrySof Natural Monofocal (Model SN60AT)
A NA study of Cataract, sponsored by Alcon Research.
- Completed
- Registry status
- NA
- Development phase
- 35
- Enrollment target
- 1
- Study location
NCT00759668 is a NA study of Cataract that has completed, run by Alcon Research. The registered enrollment target is 35 participants, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00759668, a NA study of Cataract, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- NA
- Development phase
- 35 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of the study is: * to compare visual parameters (Subjective refraction and Visual Acuity (VA)) and safety (tilt, decentration and posterior chamber opacification (PCO)) in a prospective series of 40 patients after bilateral implantation of AcrySof Natural ReSTOR (Model SN60D3) or AcrySof Natural Monofocal (Model SN60AT) * to assess patient satisfaction before and after implant
Conditions Studied
Interventions
- DEVICE Acrysof Natural ReSTOR SN60D3
- DEVICE Acrysof Natural Monofocal SN60AT
Study Locations (1)
Texas
- Contact Alcon Call Center for Trial Locations - Fort Worth
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2007-05 |
| Est. Completion | 2009-09 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00759668
The ClinicalTrials.gov registry entry for NCT00759668 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (85% lower). The listed sponsor is Alcon Research, which has 275 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Cataract appearing as the primary indexed condition, and to 2 interventions - of which Acrysof Natural ReSTOR SN60D3 is the first listed.
NCT00759668 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT00759668 about?
NCT00759668 is a clinical study titled "Visual Function and Patient Satisfaction After Bilateral Implantation of AcrySof Natural ReSTOR (Model SN60D3) or AcrySof Natural Monofocal (Model SN60AT)". The purpose of the study is: * to compare visual parameters (Subjective refraction and Visual Acuity (VA)) and safety (tilt, decentration and posterior chamber opacification (PCO)) in a prospective series of 40 patients after bilateral implantation of AcrySof Natural ReSTOR (Model SN60D3) or AcrySo...
What is the current status of trial NCT00759668?
This trial is currently completed. It is a NA study. The enrollment target is 35 participants. The study started on 2007-05. Estimated completion is 2009-09.
What conditions does trial NCT00759668 study?
This clinical trial studies the following conditions: Cataract.
What interventions are being tested in trial NCT00759668?
The interventions under investigation include: Acrysof Natural ReSTOR SN60D3 (DEVICE), Acrysof Natural Monofocal SN60AT (DEVICE).
Who is sponsoring clinical trial NCT00759668?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00759668 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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Related
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