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NCT00348205 · ClinicalTrials.gov registry record · NA
A Study to Evaluate the Safety and Effectiveness of the Technols 217z Zyoptix System for Hyperopia
A NA study of Astigmatism and Hyperopia, sponsored by Bausch & Lomb Incorporated.
- Completed
- Registry status
- NA
- Development phase
- 80
- Enrollment target
- 1
- Study location
NCT00348205 is a NA study of Astigmatism and Hyperopia that has completed, run by Bausch & Lomb Incorporated. The registered enrollment target is 80 participants, below the 104-participant average among 31 other Astigmatism trials with a reported enrollment target (23% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00348205, a NA study of Astigmatism and Hyperopia, has completed, sponsored by Bausch & Lomb Incorporated.
- COMPLETED
- Registry status
- NA
- Development phase
- 80 participants
- Enrollment target
- 1
- Study location
Study Summary
A study to demonstrate the safety and effectiveness of wavefront laser refractive surgery treatments for hyperopia and astigmatism.
Conditions Studied
Interventions
- DEVICE Technolas 217z Zyoptix Laser
Study Locations (1)
New York
- Bausch & Lomb - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2005-06 |
| Est. Completion | 2009-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00348205
The ClinicalTrials.gov registry entry for NCT00348205 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 104-participant average among 31 other Astigmatism trials with a reported enrollment target (23% lower). The listed sponsor is Bausch & Lomb Incorporated, which has 174 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Astigmatism appearing as the primary indexed condition, and to 1 intervention - of which Technolas 217z Zyoptix Laser is the first listed.
NCT00348205 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT00348205 about?
NCT00348205 is a clinical study titled "A Study to Evaluate the Safety and Effectiveness of the Technols 217z Zyoptix System for Hyperopia". A study to demonstrate the safety and effectiveness of wavefront laser refractive surgery treatments for hyperopia and astigmatism.
What is the current status of trial NCT00348205?
This trial is currently completed. It is a NA study. The enrollment target is 80 participants. The study started on 2005-06. Estimated completion is 2009-03.
What conditions does trial NCT00348205 study?
This clinical trial studies the following conditions: Astigmatism, Hyperopia.
What interventions are being tested in trial NCT00348205?
The interventions under investigation include: Technolas 217z Zyoptix Laser (DEVICE).
Who is sponsoring clinical trial NCT00348205?
This trial is sponsored by Bausch & Lomb Incorporated, which has 174 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00348205 being conducted?
This trial has 1 study location across New York. 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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