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Effect of Oxygen on results of corneal cross linking

Phase 2
Conditions
Keratoconus.
Keratoconus, unspecified, unspecified eye
H18.609
Registration Number
IRCT20140808018729N2
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

progressive KCN
Mild to moderate KCN (Kmax< 58D)
Signing informed consent form

Exclusion Criteria

Any other ocular comorbidity
Corneal thickness<450 micron

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Keratometric and topographic corneal changes. Timepoint: 0, 1, 3, 6, 12 months. Method of measurement: Refraction, pentacam, Confocal, OCT.;Pain. Timepoint: Intra operative. Method of measurement: Visual analogue scale.;Complications. Timepoint: through the course of study. Method of measurement: examination.
Secondary Outcome Measures
NameTimeMethod
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