IOL comparison study with the RALV device
- Conditions
- H25Senile cataract
- Registration Number
- DRKS00034678
- Lead Sponsor
- ACMIT Gmbh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
• Refraction: Sphere (Sph): between -3 dpt and +3 dpt
• Refraction: Cylinder (Cyl): <= 1 dpt
• Visual acuity >= 1 decimal (or <= 0 logMAR)
• After the medical examination, the subject was found suitable to receive cyclopentolate eye drops.
• Informed and signed consent to participate in the study
• Diseases that affect visual acuity (glaucoma, cataract, AMD, corneal opacity or other retinal diseases)
• Irregular astigmatism
• Previous eye surgery of any kind
• In women: pregnancy or breastfeeding
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method This is an experimental observational study with an open outcome regarding the evaluation.<br><br>The following parameters are tested:<br>• Visual acuity in FAR, INTER, NEAR distances<br>• Contrast sensitivity in FAR, INTER, NEAR distance<br>• Visual acuity defocus curves (0.5 dpt step size, +1 dpt to -4 dpt)<br>• Halo test in FAR<br>• Subjective preference tests in FAR, INTER, NEAR distance
- Secondary Outcome Measures
Name Time Method