Bilateral Cataract Clinical Trial
Official title:
Pilot Study With a Diffractive Trifocal IOL (POD AY 26P FineVision)
The principal objective of the study is to determine the visual acuity at far, intermediate and near distances tested with optotypes at different distances from the eyes and tested with defocus addition lenses of patients implanted bilaterally with the POD 26P AY FineVision. Secondary objective will be to test the glare and contrast sensitivity.
This study is a pilot study. As such it will recruit a limited number of patients : 20. Patients recruited will suffer from cataract, have no comorbidity, expressed the desire for spectacle independence and have realistic expectations. Descriptive statistics will be used to determine the visual acuities at any distance. The occurence of glare and the determination of the contrast sensitivity will also be determined. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT03861351 -
Non-comparative Trial Following Participants Implanted Bilaterally With Mini WELL Toric Ready Intraocular Lens for 6 Months After the Second Eye Implant (FUSION)
|
N/A | |
| Completed |
NCT03400124 -
Cost-effectiveness of ISBCS vs. DSBCS
|
N/A | |
| Completed |
NCT05604781 -
Symfony/Synergy IOL Combination Outcomes
|
||
| Completed |
NCT02734459 -
A Bioequivalence Study to Compare the Pharmacokinetics (PK) Of Marketed Product TobraDex® To An Experimental Ophthalmic Sterile Ointment Containing Tobramycin And Dexamethasone In Aqueous Humor In Patients Undergoing Indicated Cataract Surgery
|
Phase 3 | |
| Not yet recruiting |
NCT05069753 -
Patient Reported Visual Satisfaction Following Same Day or Delayed Bilateral Cataract Surgery
|
N/A | |
| Recruiting |
NCT05832749 -
Comparison of the Safety and Efficacy of Ophtesis Bio 3% With a Similar 3% Sodium Hyaluronate OVD
|
||
| Completed |
NCT01841957 -
Immediate Simultaneous Bilateral Cataract Surgery
|
N/A |