Study of predicted refraction error after cataract surgery using ARGOS in long and short axial length
- Conditions
- Cataract
- Registration Number
- JPRN-UMIN000043202
- Lead Sponsor
- Isanakai Medical Corporation Chukyo Eye Clinic
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 128
Not provided
(1) Patients who underwent other eye surgery within 3 months after cataract surgery (2) Patients with uncontrolled glaucoma, progressive diabetic retinopathy, uveitis, retinal detachment, iris angiogenesis, corneal degeneration, history of eye surgery including corneal transplantation and corneal refractive surgery, and severe dry eye (3) Corneal astigmatism is 2.0D or higher (4) Patients with diseases that may affect eyesight, or patients who have used drugs that may affect eyesight (5) Patients with Zinn's zonule rupture, posterior capsule breakage, vitreous prolapse, hyphema, and IOL haptics that could not be completely fixed in the lens capsule during surgery (6) Patients who the doctor deems inappropriate because of systemic or ophthalmic diseases.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method