Hyperopia Clinical Trial
Official title:
Clinical Investigation of the WaveLight® EX500 Excimer Laser for Hyperopic LASIK
The purpose of this study is to collect efficacy and safety data on the WaveLight EX500 excimer laser system for the correction of hyperopia with and without astigmatism by laser in situ keratomileusis (LASIK) treatment.
Qualified subjects will receive LASIK treatment in both eyes and be followed for 1 year. Subjects will be asked to attend a total of 9 visits (Screening, Surgery, Day 1, Week 1, Month 1, Month 3, Month 6, Month 9, and Month 12). Total expected duration of subject participation is approximately 1 year. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT06046209 -
Comparing a Monthly Replacement Lens Versus a Daily Disposable Lens
|
N/A | |
Completed |
NCT05656885 -
Clinical Evaluation of Two Frequent Replacement Soft Spherical Contact Lenses
|
N/A | |
Completed |
NCT02423109 -
Bilateral Dispensing Study of Fanfilcon A Toric Versus Enfilcon A Toric Lenses
|
N/A | |
Completed |
NCT01392950 -
Clinical Study of Clariti Monthly Contact Lens
|
N/A | |
Withdrawn |
NCT00765960 -
Evaluation of Outcomes Using the Amo Advanced CustomVue Ilasik Procedure
|
||
Completed |
NCT00520689 -
Multipurpose Disinfecting Solution Compatibility With a Silicone Hydrogel Contact Lens
|
Phase 3 | |
Completed |
NCT05538182 -
Zimbabwe Eyecare And Learning(ZEAL):Formative Research on Hyperopia and Educational Outcomes in Primary School Children
|
N/A | |
Enrolling by invitation |
NCT05976750 -
Air Optix® Night and Day® Aqua Daily Wear
|
||
Completed |
NCT02575911 -
Accuracy of LASIK Flaps Created With the LenSx® Femtosecond Laser - A Pilot Study
|
N/A | |
Completed |
NCT05735990 -
Retrospective Clinical Investigation of the Safety and Performance of 640PM Trifocal IOL Implantation in Patients With Cataract and/or Ametropia (Hyperopia, Myopia) and/or Presbyopia
|
||
Withdrawn |
NCT03671096 -
Safety and Efficacy of the Transform™ Corneal Allograft for Hyperopia Correction
|
N/A | |
Recruiting |
NCT02279446 -
Development of a Validated Chart for Intermediate Vision Assessment
|
N/A | |
Completed |
NCT02060539 -
Multicenter Dispensing Study of Biofinity Lenses in Extended Range
|
N/A | |
Completed |
NCT01951573 -
Evaluation of a New Daily Disposable Multifocal Contact Lens Design
|
N/A | |
Completed |
NCT01467557 -
Daily Disposable Performance of 1•DAY ACUVUE® TruEye™ and 1•DAY ACUVUE® MOIST® With LACREON® TECHNOLOGY
|
||
Completed |
NCT01228591 -
Pilot Dispensing Evaluation of a Plus Power Lens
|
N/A | |
Completed |
NCT03722784 -
Evaluation of Silicone Hydrogel Daily Wear Contact Lenses for Up to One (1) Month of Daily Wear
|
N/A | |
Completed |
NCT03688672 -
Apioc Contact Lens Feasibility
|
N/A | |
Completed |
NCT05741450 -
A Clinical Comparison of Two Soft Contact Lenses
|
N/A | |
Completed |
NCT01912781 -
Safety and Efficacy Evaluation of a New Contact Lens Disinfecting Solution in Gas Permeable Contact Lens Wearers
|
N/A |