A clinical study of EYECRYLâ?¢PLUS (600) intraocular lens in patients undergoing cataract surgery.
- Conditions
- Health Condition 1: H251- Age-related nuclear cataract
- Registration Number
- CTRI/2022/08/044819
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
1. Age 18 year or greater
2. Cataract
3. Calculated IOL power is within the range of the study IOLs.
4. Given consent to use device related data for scientific purpose
5. Clear intraocular media other than cataract
6. Patient willing to participate and sign informed consent
7. Patient willing to come for all post-operative follow-up
8. Female participants of child bearing potential and male participants whose partner
is of child bearing potential must be willing to ensure that they or their partner use
effective contraception during the study
1. Previous intraocular or corneal surgery
2. Traumatic cataract
3. Pregnancy
4. Concurrent participation or participation in the last 30 days in any other clinical
trial
5. Irregular astigmatism
6. Instability of keratometry or biometry measurements
7. Vulnerable subject.
8. Patients receiving chloroquine treatment.
9. Patient having Microphthalmia.
10. Patient having Chronic Uveitis.
11. Patient suffering from corneal dystrophy or endothelial insufficiency.
12. Patient having active ocular diseases (active diabetic retinopathy, uncontrolled
glaucoma)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method