Study of the Keraring Intrastromal Corneal Ring SG model
- Conditions
- KeratoconusC11.204
- Registration Number
- RBR-3dzmnn6
- Lead Sponsor
- Mediphacos Indústrias Médicas S.A.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Patients diagnosed with keratoconus; Keratoconus in contact lens-intolerant patients; Pellucid marginal degeneration; decentralization of the highest posterior elevation point = 1.25mm from the center; Keratometry with a maximum mean K of 58µm; Minimum corneal thickness of 420 µm in the 5mm optical zone; both sexes; adults and children; Patients willing and able to perform clinical examinations for follow-up for a period of 1 year after surgery
Patients with no indication for the treatment of intrastromal ring implantation; vulnerable groups
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method