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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 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 33 participants.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02060461
The ClinicalTrials.gov registry entry for NCT02060461 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which FS200 femtosecond laser LASIK is the first listed.
NCT02060461 reports 0 study locations.
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.
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