se of synthetic cornea for treatment of Keratoconus
Not Applicable
- Conditions
- Health Condition 1: H186- Keratoconus
- Registration Number
- CTRI/2023/07/055136
- Lead Sponsor
- Rajendra Prasad Centre for Ophthalmic Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Diagnosed cases of Keratoconus
Age more than 18 years
Contact lens intolerant
Thinnest Pachymetry > 250 microns
Patients giving informed consent for surgery and willing for follow up
Exclusion Criteria
Healed hydrops
Diabetes, connective tissue disease or atopy
Pregnant or lactating patients
Patient not willing to give consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method tectonic support to cornea, change in astigmatismTimepoint: changes seen at Post operative day 1, day 7, at 4 weeks and 3month
- Secondary Outcome Measures
Name Time Method change in lower order aberrations and higher order aberrations of corneaTimepoint: changes seen at Post operative day 1, day 7, at 4 weeks and 3month