Comparison of visual outcome between two different Intraocular injections for swelling of nerve tissue of eye in patients with Intraocular lens
Phase 4
- Conditions
- Health Condition 1: H350- Background retinopathy and retinalvascular changes
- Registration Number
- CTRI/2022/03/040844
- Lead Sponsor
- Il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Central subfield retinal thickness of at least 300um measured by OCT
2. Centre involving macular edema
3. Visual acuity between 6/9 to 6/60
Exclusion Criteria
1. Previous treatment in terms of : -
a) Focal/macular photocoagulation
b) Previous intravitreal injection therapy - Last 3 months
c) PRP in the last 6 months
2. Any medial opacity obscuring the fundus view
3. Intra ocular pressure >21mmHg or previous steroid responders
4. Cataract surgery and YAG capsulotomy in the last 3 months
5. PDRP patients requiring simultaneous pan-retinal photocoagulation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measurement and comparison of average threshold for macular sensitivity via microperimetry between the two treatment arms <br/ ><br>Timepoint: 0, 1, 6 month <br/ ><br>
- Secondary Outcome Measures
Name Time Method Measurement and comparison of VA (snellenâ??s 3 metre), CSRT (OCT), fixation characteristics (microperimetry) and number of injections given between the two treatment arms <br/ ><br>Timepoint: 0, 1, 6 month