Status:
COMPLETED
Clinical Investigation of OMEGA Gemini Capsule, Model Gemini IV With an Approved Monofocal or Toric IOL
Lead Sponsor:
Omega Ophthalmics
Conditions:
Cataract
Eligibility:
All Genders
40+ years
Phase:
NA
Brief Summary
This study is a prospective, randomized, controlled, paired eye, subject-masked design.
Detailed Description
Subjects will be randomly assigned to which eye will receive the Omega capsule Gemini IV with an approved monofocal or Toric intraocular lens. Fellow eyes will receive an approved monofocal or Toric I...
Eligibility Criteria
Inclusion
- 40 years of age or older at the time of surgery diagnosed with bilateral cataracts
- Able to understand and sign an informed consent
- Willing and able to complete all study visits and assessments required for the study
- Calculated lens power within the available range
- Corrected distance visual acuity is equal to or worse than 20/40 in each eye with or without a glare source present
- Bilateral cataracts eligible for extraction by phacoemulsification and capsular bag fixated IOL implantation
- Potential postop visual acuity of 20/25 or better in the judgment of the surgeon
- Preoperative corneal astigmatism of 4.0 D or less with normal corneal topography
- Clear intraocular media other than cataract
- Preop endothelial cell density of 2000 cells/mm2 or more
Exclusion
- Subject's best corrected vision is light perception or no light perception in either eye
- Cataract opacification preventing adequate Binocular Indirect Ophthalmoscopic retinal and macular examination.
- Orbital abnormalities, such as thyroid related orbitopathy, causing significant exophthalmos.
- Eyelid abnormalities causing lagophthalmos.
- Significant anterior blepharitis or meibomian gland dysfunction
- Corneal abnormalities or conditions, other than regular topographic corneal astigmatism
- Krukenburg's spindle (linear pigmentary deposits on the corneal endothelium)
- Abnormalities of the iris including trans-illumination defects
- Pupil abnormalities (abnormally shaped, fixed or non-reactive)
- Pharmacologic dilation less than 7 mm
- Axial length \<22.5mm
- Lens thickness \<4.1 mm
- Anterior chamber depth \>2.8mm
- Extremely shallow anterior chamber \<2.0mm
- Prior ocular surgery
- Epiretinal membrane
- Macular edema
- Retinal tears including operculated holes
- Amblyopia
- Glaucoma of any kind
- Pseudoexfoliation syndrome
- History of uveitis/iritis
- Diabetic retinopathy
- Acute, chronic or uncontrolled systemic or ocular disease that may confound the results of the study (including rheumatologic conditions such as Rheumatoid arthritis, ankylosing spondyliltis, Sjögren's syndrome, and neurologic conditions such as optic neuritis or multiple sclerosis).
- Prior or anticipated use of tamsulosin or silodosin (e.g., Flomax, Flomaxtra, Rapaflo) or similar medications
- Average Keratometry \<38D or \> 48D by topography
- Any pathology of the zonules including evidence of zonular weakness, zonular instability, zonular damage, or coloboma effecting zonules.
- History of ocular trauma
- Pregnant, lactating, or has another condition with associated fluctuation of hormones that could lead to refractive changes
Key Trial Info
Start Date :
February 21 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 28 2020
Estimated Enrollment :
6 Patients enrolled
Trial Details
Trial ID
NCT04058314
Start Date
February 21 2020
End Date
August 28 2020
Last Update
September 16 2020
Active Locations (1)
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1
Clinica 20/20
San José, Costa Rica