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NCT02060461 · ClinicalTrials.gov registry record · NA
LASIK Flap Thickness and Visual Outcomes Using the WaveLight FS200 Femtosecond Laser
A NA study, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 33
- Enrollment target
NCT02060461: Completed NA study, sponsored by The Cleveland Clinic.
NCT02060461 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 33 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02060461, a NA study, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 33 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the visual outcome, accuracy, predictability and complications of LASIK flap creation using the Alcon Wavelight FS200 Femtosecond laser and compare these results to those obtained using current IntraLase FS60 Femtosecond laser. The primary outcome to be evaluated is the flap thickness accuracy.
Primary Outcome
Central LASIK flap thickness for each femtosecond laser. Each treatment was set for a 110 micrometer thick flap.
Interventions
- DEVICE FS200 femtosecond laser LASIK
- DEVICE IntraLase femtosecond laser LASIK
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2012-08 |
| Est. Completion | 2016-09 |
| Phase | NA |
What the finished NCT02060461 record still lists
NCT02060461 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 2 interventions - of which FS200 femtosecond laser LASIK is the first listed.
NCT02060461 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02060461 about?
NCT02060461 is a clinical study titled "LASIK Flap Thickness and Visual Outcomes Using the WaveLight FS200 Femtosecond Laser". The objective of this study is to evaluate the visual outcome, accuracy, predictability and complications of LASIK flap creation using the Alcon Wavelight FS200 Femtosecond laser and compare these results to those obtained using current IntraLase FS60 Femtosecond laser. The primary outcome to be eva...
What is the current status of trial NCT02060461?
This trial is currently completed. It is a NA study. The enrollment target is 33 participants. The study started on 2012-08. Estimated completion is 2016-09.
What interventions are being tested in trial NCT02060461?
The interventions under investigation include: FS200 femtosecond laser LASIK (DEVICE), IntraLase femtosecond laser LASIK (DEVICE).
Who is sponsoring clinical trial NCT02060461?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02060461's enrollment target sits among peer trials
33 1574th of 2000 higher than 423 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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