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Study of the Keraring Intrastromal Corneal Ring SG model

Not Applicable
Recruiting
Conditions
Keratoconus
C11.204
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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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